A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739220



Internal ID162886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10309170..10311077hg38UCSC Ensembl
chrX:10277210..10279117hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381908
hg191908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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