A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582369



Internal ID16023092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:85698544..85699019hg38UCSC Ensembl
Innerchr2:85925667..85926142hg19UCSC Ensembl
Innerchr2:85779178..85779653hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38476
hg19476
hg18476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913829
Samples
Known GenesGNLY
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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