A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520197



Internal ID15447490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23033043..23081799hg38UCSC Ensembl
InnerchrX:23051160..23099916hg19UCSC Ensembl
InnerchrX:22961081..23009837hg18UCSC Ensembl
InnerchrX:22810817..22859573hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3848757
hg1948757
hg1848757
hg1748757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661646, nssv673646
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520197
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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