A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110032



Internal ID15963218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374115..39472638hg38UCSC Ensembl
Innerchr8:39231634..39330157hg19UCSC Ensembl
Innerchr8:39350791..39449314hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3898524
hg1998524
hg1898524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610959
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110032
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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