A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581799



Internal ID16369208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49292196..49433197hg38UCSC Ensembl
Innerchr2:49519335..49660335hg19UCSC Ensembl
Innerchr2:49372839..49513839hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38141002
hg19141001
hg18141001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6857n54
Supporting Variantsnssv908245
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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