A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740185



Internal ID163851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55036600..55048964hg38UCSC Ensembl
chrX:55063033..55075397hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3812365
hg1912365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000417973


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