A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520696



Internal ID20894057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34273401..34276200hg38UCSC Ensembl
chr18:31853365..31856164hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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