A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581744



Internal ID16369153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46409942..46433613hg38UCSC Ensembl
Innerchr2:46637081..46660752hg19UCSC Ensembl
Innerchr2:46490585..46514256hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3823672
hg1923672
hg1823672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150439
SamplesNINDS_163
Known GenesLOC101805491
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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