A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581710



Internal ID16369119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45253003..45298301hg38UCSC Ensembl
Innerchr2:45480142..45525440hg19UCSC Ensembl
Innerchr2:45333646..45378944hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3845299
hg1945299
hg1845299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6841n54
Supporting Variantsnssv1150434
Samples1798860279_A
Known GenesLINC01121
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581710
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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