A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344773



Internal ID21002326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167296915..167297355hg38UCSC Ensembl
chr2:168153425..168153865hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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