A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737768



Internal ID161434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146043082..146053609hg38UCSC Ensembl
chrX:145124600..145135127hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3810528
hg1910528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737768
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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