A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581868



Internal ID16022591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51053379..51125305hg38UCSC Ensembl
Innerchr2:51280517..51352443hg19UCSC Ensembl
Innerchr2:51134021..51205947hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3871927
hg1971927
hg1871927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908396
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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