A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528469



Internal ID15109076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:19500814..19522930hg38UCSC Ensembl
InnerchrX:19518932..19541048hg19UCSC Ensembl
InnerchrX:19428853..19450969hg18UCSC Ensembl
InnerchrX:19278589..19300705hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3822117
hg1922117
hg1822117
hg1722117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705072
Samples
Known GenesMAP3K15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528469
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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