A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582344



Internal ID16369753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81507668..81761258hg38UCSC Ensembl
Innerchr2:81734792..81988382hg19UCSC Ensembl
Innerchr2:81588303..81841893hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38253591
hg19253591
hg18253591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913801
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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