A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv515n21



Internal ID22766707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69166020..69180698hg38UCSC Ensembl
chrX:68385863..68400541hg19UCSC Ensembl
chrX:68302588..68317266hg18UCSC Ensembl
chrX:68168884..68183562hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3814679
hg1914679
hg1814679
hg1714679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524851, nsv518868
Samples
Known GenesLINC00269
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv515n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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