A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534079



Internal ID20907440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35238001..35243300hg38UCSC Ensembl
chr18:32817965..32823264hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191436
Samples
Known GenesZNF397
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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