A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997365



Internal ID19156903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58848323..58930257hg38UCSC Ensembl
Innerchr3:58834049..58915983hg19UCSC Ensembl
Innerchr3:58809089..58891023hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3881935
hg1981935
hg1881935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593393
Samples
Known GenesC3orf67
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997365
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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