A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582359



Internal ID16369768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83001127..83123080hg38UCSC Ensembl
Innerchr2:83228251..83350204hg19UCSC Ensembl
Innerchr2:83081762..83203715hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38121954
hg19121954
hg18121954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6944n54
Supporting Variantsnssv1150781
SamplesNINDS_44
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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