A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522994



Internal ID20896355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:807302..811167hg38UCSC Ensembl
chr18:807303..811168hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg383866
hg193866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044075
Samples
Known GenesYES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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