A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440604



Internal ID22498474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109109985..109114179hg38UCSC Ensembl
chrX:108353215..108357409hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg384195
hg194195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440604
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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