A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581553



Internal ID16368962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41003722..41128308hg38UCSC Ensembl
Innerchr2:41230862..41355448hg19UCSC Ensembl
Innerchr2:41084366..41208952hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38124587
hg19124587
hg18124587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6810n54
Supporting Variantsnssv906974
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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