A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453841



Internal ID22511716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70373622..70373727hg38UCSC Ensembl
chrX:69593472..69593577hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886324
Supporting Variants
Samples
Known GenesKIF4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453841
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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