A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv517n21



Internal ID20132238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78406942..78868581hg38UCSC Ensembl
chrX:77662439..78124078hg19UCSC Ensembl
chrX:77549095..78010734hg18UCSC Ensembl
chrX:77468584..77930223hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38461640
hg19461640
hg18461640
hg17461640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528728, nsv521599
Samples
Known GenesLPAR4, ZCCHC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv517n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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