A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003249



Internal ID19092467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65222026..65252682hg38UCSC Ensembl
Innerchr3:65207701..65238357hg19UCSC Ensembl
Innerchr3:65182741..65213397hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3830657
hg1930657
hg1830657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593954
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)nsv1003249
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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