A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043282



Internal ID20610322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6691534..6697315hg38UCSC Ensembl
chr18:6691533..6697314hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385782
hg195782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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