A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362693



Internal ID21020246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84614101..84670700hg38UCSC Ensembl
chr3:84663252..84719851hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3856600
hg1956600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210116
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362693
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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