A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666677



Internal ID15403329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184471845..184476333hg38UCSC Ensembl
Innerchr3:184189633..184194121hg19UCSC Ensembl
Innerchr3:185672327..185676815hg18UCSC Ensembl
Innerchr3:185672335..185676823hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg384489
hg194489
hg184489
hg174489
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516188
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666677
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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