A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693482



Internal ID15083448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152109627..152136472hg38UCSC Ensembl
InnerchrX:151278099..151304944hg19UCSC Ensembl
InnerchrX:151028755..151055600hg18UCSC Ensembl
InnerchrX:150948667..150975512hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3826846
hg1926846
hg1826846
hg1726846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520971
Supporting Variants
Samples
Known GenesMAGEA10, MAGEA10-MAGEA5, MAGEA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693482
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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