A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437314



Internal ID15382620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207488339..207493114hg38UCSC Ensembl
Outerchr2:207484534..207498338hg38UCSC Ensembl
Innerchr2:208353063..208357838hg19UCSC Ensembl
Outerchr2:208349258..208363062hg19UCSC Ensembl
Innerchr2:208061308..208066083hg18UCSC Ensembl
Outerchr2:208057503..208071307hg18UCSC Ensembl
Innerchr2:208555606..208560381hg16UCSC Ensembl
Outerchr2:208551801..208565605hg16UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3813805
hg1913805
hg1813805
hg1613805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467195
SamplesNA18854
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)nsv437314
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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