A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706097



Internal ID15442749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108162476..108166537hg38UCSC Ensembl
Innerchr13:108814824..108818885hg19UCSC Ensembl
Innerchr13:107612825..107616886hg18UCSC Ensembl
Innerchr13:107612825..107616886hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384062
hg194062
hg184062
hg174062
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522687
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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