A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680977



Internal ID15417629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183904203..183916804hg38UCSC Ensembl
Innerchr3:183621991..183634592hg19UCSC Ensembl
Innerchr3:185104685..185117286hg18UCSC Ensembl
Innerchr3:185104693..185117294hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3812602
hg1912602
hg1812602
hg1712602
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515691
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680977
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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