A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152281



Internal ID18850488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:109647670..109651171hg38UCSC Ensembl
OuterchrX:108890899..108894400hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383502
hg193502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996885
SamplesKWB1
Known GenesACSL4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152281
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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