A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv504n21



Internal ID20132225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24115349..24216380hg38UCSC Ensembl
chrX:24133466..24234497hg19UCSC Ensembl
chrX:24043387..24144418hg18UCSC Ensembl
chrX:23893123..23994154hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38101032
hg19101032
hg18101032
hg17101032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522378, nsv516667
Samples
Known GenesZFX, ZFX-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv504n21
Frequency
Sample Size2026
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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