A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582396



Internal ID16369805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89026617..90226525hg38UCSC Ensembl
Innerchr2:89326114..90265391hg19UCSC Ensembl
Innerchr2:89107229..89902696hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381199909
hg19939278
hg18795468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6950n54
Supporting Variantsnssv913926
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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