A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739111



Internal ID162777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7368700..7393488hg38UCSC Ensembl
chrX:7286741..7311529hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3824789
hg1924789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428072
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000209074


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