A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146877



Internal ID18848760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155299986..155303787hg38UCSC Ensembl
OuterchrX:154529299..154533100hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383802
hg193802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998242
SamplesKWB1
Known GenesCLIC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146877
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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