A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522594



Internal ID15103201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:41104874..41238429hg38UCSC Ensembl
InnerchrX:40964127..41097682hg19UCSC Ensembl
InnerchrX:40849071..40982626hg18UCSC Ensembl
InnerchrX:40720381..40853936hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38133556
hg19133556
hg18133556
hg17133556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv512n21
Supporting Variantsnssv705984
Samples
Known GenesUSP9X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522594
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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