A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv512n21



Internal ID20132233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41104874..41269240hg38UCSC Ensembl
chrX:40964127..41128493hg19UCSC Ensembl
chrX:40849071..41013437hg18UCSC Ensembl
chrX:40720381..40884747hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38164367
hg19164367
hg18164367
hg17164367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516661, nsv522594
Samples
Known GenesUSP9X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv512n21
Frequency
Sample Size2026
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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