A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582051



Internal ID16369460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56479623..56675574hg38UCSC Ensembl
Innerchr2:56706758..56902709hg19UCSC Ensembl
Innerchr2:56560262..56756213hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38195952
hg19195952
hg18195952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6897n54
Supporting Variantsnssv911173
Samples
Known GenesRNU6-35P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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