A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523726



Internal ID15451019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33540611..33711285hg38UCSC Ensembl
InnerchrX:33558728..33729402hg19UCSC Ensembl
InnerchrX:33468649..33639323hg18UCSC Ensembl
InnerchrX:33318385..33489059hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38170675
hg19170675
hg18170675
hg17170675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699542
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523726
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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