A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352364



Internal ID22294959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79816718..79817023hg38UCSC Ensembl
chrX:79072215..79072520hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208598
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352364
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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