A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702077



Internal ID15092043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26225590..26768819hg38UCSC Ensembl
InnerchrX:26243707..26786936hg19UCSC Ensembl
InnerchrX:26153628..26696857hg18UCSC Ensembl
InnerchrX:26003364..26546593hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38543230
hg19543230
hg18543230
hg17543230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525877
Supporting Variants
Samples
Known GenesVENTXP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702077
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