A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959328



Internal ID19210378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:54431604..54431656hg38UCSC Ensembl
OuterchrX:54458037..54458089hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110083
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959328
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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