A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1120778



Internal ID15973964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127484261..127519628hg38UCSC Ensembl
Innerchr8:128496506..128531873hg19UCSC Ensembl
Innerchr8:128565688..128601055hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3835368
hg1935368
hg1835368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1120778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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