A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437522



Internal ID15382828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112835967..112839273hg38UCSC Ensembl
Outerchr6:112830861..112857832hg38UCSC Ensembl
Innerchr6:113157169..113160475hg19UCSC Ensembl
Outerchr6:113152063..113179034hg19UCSC Ensembl
Innerchr6:113263862..113267168hg18UCSC Ensembl
Outerchr6:113258756..113285727hg18UCSC Ensembl
Innerchr6:113202739..113206045hg16UCSC Ensembl
Outerchr6:113197633..113224604hg16UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3826972
hg1926972
hg1826972
hg1626972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467403
SamplesNA19100
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)nsv437522
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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