A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694597



Internal ID15431249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131151452..131197840hg38UCSC Ensembl
InnerchrX:130285426..130331814hg19UCSC Ensembl
InnerchrX:130113107..130159495hg18UCSC Ensembl
InnerchrX:130010961..130057349hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3846389
hg1946389
hg1846389
hg1746389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517789
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694597
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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