A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988456



Internal ID19222746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:109556805..109556879hg38UCSC Ensembl
OuterchrX:108800034..108800108hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134938
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988456
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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