A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697335



Internal ID15433987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98642128..98841415hg38UCSC Ensembl
InnerchrX:97897126..98096413hg19UCSC Ensembl
InnerchrX:97783782..97983069hg18UCSC Ensembl
InnerchrX:97703271..97902558hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38199288
hg19199288
hg18199288
hg17199288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520300
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697335
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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