A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581485



Internal ID16022208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38612181..38666518hg38UCSC Ensembl
Innerchr2:38839323..38893660hg19UCSC Ensembl
Innerchr2:38692827..38747164hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3854338
hg1954338
hg1854338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv906875
Samples
Known GenesGALM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581485
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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