A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696662



Internal ID15086628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85666713..85763620hg38UCSC Ensembl
InnerchrX:84921718..85018625hg19UCSC Ensembl
InnerchrX:84808374..84905281hg18UCSC Ensembl
InnerchrX:84727863..84824770hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3896908
hg1996908
hg1896908
hg1796908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519786
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696662
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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