A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526002



Internal ID15453295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90571814..90610046hg38UCSC Ensembl
Innerchr13:91224068..91262300hg19UCSC Ensembl
Innerchr13:90022069..90060301hg18UCSC Ensembl
Innerchr13:90022069..90060301hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3838233
hg1938233
hg1838233
hg1738233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702228
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526002
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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