A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398802



Internal ID21056355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73152201..73164100hg38UCSC Ensembl
chr6:73861924..73873823hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229912
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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