A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697303



Internal ID15433955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93398386..93447359hg38UCSC Ensembl
InnerchrX:92653385..92702358hg19UCSC Ensembl
InnerchrX:92540041..92589014hg18UCSC Ensembl
InnerchrX:92459530..92508503hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3848974
hg1948974
hg1848974
hg1748974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697303
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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