A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435958



Internal ID22493828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113181466..113181746hg38UCSC Ensembl
chrX:112424693..112424973hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882308
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435958
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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