A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741706



Internal ID165372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101087200..101093500hg38UCSC Ensembl
chrX:100342189..100348489hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg386301
hg196301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420048
Supporting Variants
Samples
Known GenesTMEM35
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741706
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00188719


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