A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736796



Internal ID160462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47471611..47471753hg38UCSC Ensembl
chrX:47331010..47331152hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428457
Supporting Variants
Samples
Known GenesZNF41
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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