A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645931



Internal ID21837978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20146260..20146342hg38UCSC Ensembl
chrX:20164378..20164460hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645931
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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