A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156636



Internal ID15854160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95571323..95584126hg38UCSC Ensembl
Innerchr8:96583551..96596354hg19UCSC Ensembl
Innerchr8:96652727..96665530hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3812804
hg1912804
hg1812804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611763
Supporting Variants
Samples1780862001_A
Known GenesLOC100616530
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156636
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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