A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520530



Internal ID15447823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34393673..34522710hg38UCSC Ensembl
InnerchrX:34411790..34540827hg19UCSC Ensembl
InnerchrX:34321711..34450748hg18UCSC Ensembl
InnerchrX:34171447..34300484hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38129038
hg19129038
hg18129038
hg17129038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697471
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520530
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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