A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589962



Internal ID16377371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26004870..26115654hg38UCSC Ensembl
Innerchr3:26046361..26157145hg19UCSC Ensembl
Innerchr3:26021365..26132149hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38110785
hg19110785
hg18110785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8265n54
Supporting Variantsnssv960138, nssv960135, nssv960137, nssv960136
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589962
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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