A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147251



Internal ID19198397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2915158..2918259hg38UCSC Ensembl
OuterchrX:2833199..2836300hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000025
SamplesKWB1
Known GenesARSD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147251
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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