A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645211



Internal ID21837258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101056503..101247077hg38UCSC Ensembl
chrX:100311492..100502066hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38190575
hg19190575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112218
Supporting Variants
Samples
Known GenesCENPI, DRP2, TMEM35
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645211
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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