A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671469



Internal ID15408121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:59079708..59089224hg38UCSC Ensembl
Innerchr13:59653842..59663358hg19UCSC Ensembl
Innerchr13:58551843..58561359hg18UCSC Ensembl
Innerchr13:58551843..58561359hg17UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg389517
hg199517
hg189517
hg179517
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520208
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671469
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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