A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437989



Internal ID22495859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109653483..109658927hg38UCSC Ensembl
chrX:108896712..108902156hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385445
hg195445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869115
Supporting Variants
Samples
Known GenesACSL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437989
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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