A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529213



Internal ID20902574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36093862..36102723hg38UCSC Ensembl
chr18:33673825..33682686hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg388862
hg198862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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