A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150046



Internal ID18854895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:152745001..152753276hg38UCSC Ensembl
OuterchrX:151910899..151921800hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg388276
hg1910902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998833
SamplesKWB1
Known GenesMAGEA2, MAGEA2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150046
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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