A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352739



Internal ID22265370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121172376..121172473hg38UCSC Ensembl
chrX:120306230..120306327hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526218
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352739
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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