A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360147



Internal ID21017700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128073801..128076000hg38UCSC Ensembl
chr3:127792644..127794843hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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