A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520388



Internal ID15100995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38257469..38303823hg38UCSC Ensembl
InnerchrX:38116722..38163076hg19UCSC Ensembl
InnerchrX:38001666..38048020hg18UCSC Ensembl
InnerchrX:37872939..37919293hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3846355
hg1946355
hg1846355
hg1746355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv510n21
Supporting Variantsnssv697386
Samples
Known GenesRPGR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520388
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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