A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582077



Internal ID16369486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57175505..57238668hg38UCSC Ensembl
Innerchr2:57402640..57465803hg19UCSC Ensembl
Innerchr2:57256144..57319307hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3863164
hg1963164
hg1863164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6900n54
Supporting Variantsnssv911230, nssv911231, nssv911226, nssv911225, nssv911227, nssv911229, nssv911228
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582077
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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