A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741801



Internal ID165467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105826249..105826307hg38UCSC Ensembl
chrX:105070242..105070300hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427345
Supporting Variants
Samples
Known GenesNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741801
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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