A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610973



Internal ID16398382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375062..39540503hg38UCSC Ensembl
Innerchr8:39232581..39398022hg19UCSC Ensembl
Innerchr8:39351738..39517179hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38165442
hg19165442
hg18165442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12095n54
Supporting Variantsnssv1110437
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610973
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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