A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352367



Internal ID22312138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79864707..79864784hg38UCSC Ensembl
chrX:79120207..79120284hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526828
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352367
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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