A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350677



Internal ID22124888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23850382..23850442hg38UCSC Ensembl
chrX:23868499..23868559hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192106
Supporting Variants
SamplesHG00512
Known GenesAPOO
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350677
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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