A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110608



Internal ID18932150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:65603020..65620621hg38UCSC Ensembl
OuterchrX:64822900..64840500hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3817602
hg1917601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960263
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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