A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354142



Internal ID21011695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182786882..182787100hg38UCSC Ensembl
chr2:183651609..183651827hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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