A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654767



Internal ID15044733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141208424..141467288hg38UCSC Ensembl
InnerchrX:140302604..140555282hg19UCSC Ensembl
InnerchrX:140130270..140382948hg18UCSC Ensembl
InnerchrX:140028124..140280802hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38258865
hg19252679
hg18252679
hg17252679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known GenesSPANXC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654767
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