A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769647



Internal ID19309687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2413558..2419959hg38UCSC Ensembl
chrX:2331599..2338000hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg386402
hg196402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078103
Supporting Variants
SamplesKWP1
Known GenesDHRSX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769647
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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