A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041668



Internal ID21950999
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 StatusM
Merged Variants
Supporting Variantsnssv17630118
Samples
Known GenesHAVCR1P1, ZNF254
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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