A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697872



Internal ID15087838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:105935140..106434204hg38UCSC Ensembl
InnerchrX:105179132..105677434hg19UCSC Ensembl
InnerchrX:105065788..105564090hg18UCSC Ensembl
InnerchrX:104985277..105483579hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38499065
hg19498303
hg18498303
hg17498303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521259
Supporting Variants
Samples
Known GenesMUM1L1, NRK, SERPINA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697872
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