A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737371



Internal ID161037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120296566..120297170hg38UCSC Ensembl
chrX:119430421..119431025hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415786
Supporting Variants
Samples
Known GenesTMEM255A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.020762


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