A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408904



Internal ID21066457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27509601..27736330hg38UCSC Ensembl
chr6:27477380..27704109hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38226730
hg19226730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232494
Samples
Known GenesLINC01012
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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