A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705250



Internal ID15441902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118657993..118698404hg38UCSC Ensembl
InnerchrX:117791956..117832367hg19UCSC Ensembl
InnerchrX:117675984..117716395hg18UCSC Ensembl
InnerchrX:117573838..117614249hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3840412
hg1940412
hg1840412
hg1740412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517257
Supporting Variants
Samples
Known GenesDOCK11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705250
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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