A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668663



Internal ID15405315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40138804..40146857hg38UCSC Ensembl
Innerchr13:40712941..40720994hg19UCSC Ensembl
Innerchr13:39610941..39618994hg18UCSC Ensembl
Innerchr13:39610941..39618994hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg388054
hg198054
hg188054
hg178054
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516486
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668663
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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