A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675265



Internal ID15065231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62725627..62728634hg38UCSC Ensembl
Innerchr3:62711302..62714309hg19UCSC Ensembl
Innerchr3:62686342..62689349hg18UCSC Ensembl
Innerchr3:62686342..62689349hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg383008
hg193008
hg183008
hg173008
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517777
Supporting Variants
Samples
Known GenesCADPS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675265
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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