A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684040



Internal ID15420692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33373627..33476588hg38UCSC Ensembl
InnerchrX:33391744..33494705hg19UCSC Ensembl
InnerchrX:33301665..33404626hg18UCSC Ensembl
InnerchrX:33151401..33254362hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38102962
hg19102962
hg18102962
hg17102962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516480
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684040
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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