A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685190



Internal ID15421842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69916258..69973680hg38UCSC Ensembl
InnerchrX:69136101..69193530hg19UCSC Ensembl
InnerchrX:69052826..69110255hg18UCSC Ensembl
InnerchrX:68919122..68976551hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3857423
hg1957430
hg1857430
hg1757430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520990
Supporting Variants
Samples
Known GenesEDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685190
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer