A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518696



Internal ID20892057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71563401..71564200hg38UCSC Ensembl
chr18:69230637..69231436hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042847
Samples
Known GenesLOC100505776
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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