A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611026



Internal ID16398435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39393511..39480405hg38UCSC Ensembl
Innerchr8:39251030..39337924hg19UCSC Ensembl
Innerchr8:39370187..39457081hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3886895
hg1986895
hg1886895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12096n54
Supporting Variantsnssv1111112, nssv1111110, nssv1111111
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611026
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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