A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111232



Internal ID15964418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39483411..39529660hg38UCSC Ensembl
Innerchr8:39340930..39387179hg19UCSC Ensembl
Innerchr8:39460087..39506336hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3846250
hg1946250
hg1846250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611069
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111232
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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