A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352147



Internal ID21009700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206040266..206042923hg38UCSC Ensembl
chr2:206904990..206907647hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082937
Samples
Known GenesINO80D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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