A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695079



Internal ID15431731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123074675..123117143hg38UCSC Ensembl
InnerchrX:122208528..122250996hg19UCSC Ensembl
InnerchrX:122036209..122078677hg18UCSC Ensembl
InnerchrX:121934063..121976531hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3842469
hg1942469
hg1842469
hg1742469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522298
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695079
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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