A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696436



Internal ID15433088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95485632..95576251hg38UCSC Ensembl
InnerchrX:94740631..94831250hg19UCSC Ensembl
InnerchrX:94627287..94717906hg18UCSC Ensembl
InnerchrX:94546776..94637395hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3890620
hg1990620
hg1890620
hg1790620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518968
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696436
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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