A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610956



Internal ID16398365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39367449..39532700hg38UCSC Ensembl
Innerchr8:39224968..39390219hg19UCSC Ensembl
Innerchr8:39344125..39509376hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38165252
hg19165252
hg18165252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12095n54
Supporting Variantsnssv1110028, nssv1110029
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610956
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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