A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349864



Internal ID22277004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10032831..10032980hg38UCSC Ensembl
chrX:10000871..10001020hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203513
Supporting Variants
SamplesNA19239
Known GenesWWC3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349864
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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