A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664625



Internal ID15401277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8956882..8989353hg38UCSC Ensembl
InnerchrX:8924923..8957394hg19UCSC Ensembl
InnerchrX:8884923..8917394hg18UCSC Ensembl
InnerchrX:8734659..8767130hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3832472
hg1932472
hg1832472
hg1732472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515590
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664625
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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