A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741887



Internal ID165553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108364708..108379725hg38UCSC Ensembl
chrX:107607938..107622955hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3815018
hg1915018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137873
Supporting Variants
Samples
Known GenesCOL4A6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741887
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00228928


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