A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581835



Internal ID16369244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49531537..49634996hg38UCSC Ensembl
Innerchr2:49758675..49862134hg19UCSC Ensembl
Innerchr2:49612179..49715638hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38103460
hg19103460
hg18103460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150214
Samples1780854467_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581835
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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