A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435353



Internal ID22493223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112917194..112925709hg38UCSC Ensembl
chrX:112160422..112168937hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg388516
hg198516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435353
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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