A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701310



Internal ID15091276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131344926..131346274hg38UCSC Ensembl
InnerchrX:130478900..130480248hg19UCSC Ensembl
InnerchrX:130306581..130307929hg18UCSC Ensembl
InnerchrX:130204435..130205783hg17UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg381349
hg191349
hg181349
hg171349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520550
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701310
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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