A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999632



Internal ID19192995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:65618220..65620621hg38UCSC Ensembl
OuterchrX:64838099..64840500hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146429
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999632
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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