A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524257



Internal ID20897618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70461147..70504418hg38UCSC Ensembl
chr18:68128383..68171654hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3843272
hg1943272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524257
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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