A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010176



Internal ID19099394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80485195..80606209hg38UCSC Ensembl
Innerchr3:80534345..80655360hg19UCSC Ensembl
Innerchr3:80617035..80738050hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38121015
hg19121016
hg18121016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596233
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010176
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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