A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528126



Internal ID15455419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82741517..82782430hg38UCSC Ensembl
Innerchr13:83315652..83356565hg19UCSC Ensembl
Innerchr13:82213653..82254566hg18UCSC Ensembl
Innerchr13:82213653..82254566hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3840914
hg1940914
hg1840914
hg1740914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704671
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528126
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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