A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742568



Internal ID166234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137103946..137124090hg38UCSC Ensembl
chrX:136186105..136206249hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3820145
hg1920145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0024974


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