A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702585



Internal ID15439237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121592653..121954738hg38UCSC Ensembl
InnerchrX:120726507..121088591hg19UCSC Ensembl
InnerchrX:120554188..120916272hg18UCSC Ensembl
InnerchrX:120452042..120814126hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38362086
hg19362085
hg18362085
hg17362085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526303
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702585
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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