A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610955



Internal ID16398364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39367449..39520881hg38UCSC Ensembl
Innerchr8:39224968..39378400hg19UCSC Ensembl
Innerchr8:39344125..39497557hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38153433
hg19153433
hg18153433
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12094n54
Supporting Variantsnssv1110025, nssv1110027, nssv1110026, nssv1110024
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610955
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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