A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517880



Internal ID20891241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70429552..70497164hg38UCSC Ensembl
chr18:68096788..68164400hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3867613
hg1967613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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