A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704499



Internal ID15441151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:146505451..146569201hg38UCSC Ensembl
InnerchrX:145586969..145650719hg19UCSC Ensembl
InnerchrX:145394661..145458411hg18UCSC Ensembl
InnerchrX:145292515..145356265hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3863751
hg1963751
hg1863751
hg1763751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527981
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704499
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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