A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525759



Internal ID15106366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101716913..101718160hg38UCSC Ensembl
Innerchr13:102369263..102370510hg19UCSC Ensembl
Innerchr13:101167264..101168511hg18UCSC Ensembl
Innerchr13:101167264..101168511hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381248
hg191248
hg181248
hg171248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701927
Samples
Known GenesITGBL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525759
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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