A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554581



Internal ID21878936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44374051..44375531hg38UCSC Ensembl
chr4:44376068..44377548hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg381481
hg191481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997711
Supporting Variants
Samples
Known GenesKCTD8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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