A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657545



Internal ID15394197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96535820..96572530hg38UCSC Ensembl
InnerchrX:95790819..95827529hg19UCSC Ensembl
InnerchrX:95677475..95714185hg18UCSC Ensembl
InnerchrX:95596964..95633674hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3836711
hg1936711
hg1836711
hg1736711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519679
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657545
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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