A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736658



Internal ID160324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44477160..44482421hg38UCSC Ensembl
chrX:44336406..44341667hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg385262
hg195262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000832466


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