A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396022



Internal ID21053575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63450235..63455627hg38UCSC Ensembl
chr6:64160140..64165532hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg385393
hg195393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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