A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699147



Internal ID15435799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75478991..75481744hg38UCSC Ensembl
Innerchr3:75528142..75530895hg19UCSC Ensembl
Innerchr3:75610832..75613585hg18UCSC Ensembl
Innerchr3:75610832..75613585hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382754
hg192754
hg182754
hg172754
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699147
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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