A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630118



Internal ID21822165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23973910..24177467hg38UCSC Ensembl
chr19:24156712..24360269hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38203558
hg19203558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041668
Supporting Variants
Samples
Known GenesHAVCR1P1, ZNF254
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630118
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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