A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682652



Internal ID15419304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40138804..40144543hg38UCSC Ensembl
Innerchr13:40712941..40718680hg19UCSC Ensembl
Innerchr13:39610941..39616680hg18UCSC Ensembl
Innerchr13:39610941..39616680hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg385740
hg195740
hg185740
hg175740
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)nssv682652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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