A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978392



Internal ID19244333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:110596972..110612172hg38UCSC Ensembl
OuterchrX:109840200..109855400hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3815201
hg1915201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140056
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978392
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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