A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436376



Internal ID22494246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122843719..122843823hg38UCSC Ensembl
chrX:121977572..121977676hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436376
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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