A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679486



Internal ID15069452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:41202611..41217942hg38UCSC Ensembl
InnerchrX:41061864..41077195hg19UCSC Ensembl
InnerchrX:40946808..40962139hg18UCSC Ensembl
InnerchrX:40818118..40833449hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3815332
hg1915332
hg1815332
hg1715332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516661
Supporting Variants
Samples
Known GenesUSP9X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679486
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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