A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769404



Internal ID19305112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19143081..19147782hg38UCSC Ensembl
chrX:19161199..19165900hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077578
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769404
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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