A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959795



Internal ID19223462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:107364770..107370870hg38UCSC Ensembl
OuterchrX:106608000..106614100hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119355
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959795
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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