A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581567



Internal ID16368976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41011504..41048432hg38UCSC Ensembl
Innerchr2:41238644..41275572hg19UCSC Ensembl
Innerchr2:41092148..41129076hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3836929
hg1936929
hg1836929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6809n54
Supporting Variantsnssv907333, nssv907332, nssv907331
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581567
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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