A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119373



Internal ID18905299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155516239..155518939hg38UCSC Ensembl
OuterchrX:154745900..154748600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382701
hg192701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959813
SamplesKWS1
Known GenesTMLHE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119373
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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