A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703917



Internal ID15440569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70706792..70824730hg38UCSC Ensembl
InnerchrX:69926642..70044580hg19UCSC Ensembl
InnerchrX:69843367..69961305hg18UCSC Ensembl
InnerchrX:69709663..69827601hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38117939
hg19117939
hg18117939
hg17117939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517078
Supporting Variants
Samples
Known GenesTEX11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703917
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