A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353425



Internal ID22195016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123725617..123726513hg38UCSC Ensembl
chrX:122859467..122860363hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202532
Supporting Variants
SamplesHG00731
Known GenesTHOC2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353425
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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