A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959770



Internal ID19216919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:18106480..18110580hg38UCSC Ensembl
OuterchrX:18124600..18128700hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119332
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959770
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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