A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582175



Internal ID16369584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:69763158..69820512hg38UCSC Ensembl
Innerchr2:69990290..70047644hg19UCSC Ensembl
Innerchr2:69843794..69901148hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3857355
hg1957355
hg1857355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911680
Samples
Known GenesANXA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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