A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525038



Internal ID15452331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121583547..121820265hg38UCSC Ensembl
InnerchrX:120717401..120954118hg19UCSC Ensembl
InnerchrX:120545082..120781799hg18UCSC Ensembl
InnerchrX:120442936..120679653hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38236719
hg19236718
hg18236718
hg17236718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv529n21
Supporting Variantsnssv701082
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525038
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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