A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351585



Internal ID22159704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730207..9730377hg38UCSC Ensembl
chrX:9698247..9698417hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526135
Supporting Variants
SamplesHG00514
Known GenesGPR143
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351585
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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