A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150454



Internal ID18853041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:19939581..19946182hg38UCSC Ensembl
OuterchrX:19957699..19964300hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg386602
hg196602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003754
SamplesKWB1
Known GenesCXorf23
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150454
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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