A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437606



Internal ID15382912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:24643049..24652504hg38UCSC Ensembl
Outerchr8:24642997..24652865hg38UCSC Ensembl
Innerchr8:24500562..24510017hg19UCSC Ensembl
Outerchr8:24500510..24510378hg19UCSC Ensembl
Innerchr8:24556452..24565907hg18UCSC Ensembl
Outerchr8:24556400..24566268hg18UCSC Ensembl
Innerchr8:24522445..24531900hg16UCSC Ensembl
Outerchr8:24522393..24532261hg16UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg389869
hg199869
hg189869
hg169869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467487
SamplesNA19221
Known Genes
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437606
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer