A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658678



Internal ID15395330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245608..149255678hg38UCSC Ensembl
Innerchr3:148963395..148973465hg19UCSC Ensembl
Innerchr3:150446085..150456155hg18UCSC Ensembl
Innerchr3:150446093..150456163hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3810071
hg1910071
hg1810071
hg1710071
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515663
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658678
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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