A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142846



Internal ID20709886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33536659..33542594hg38UCSC Ensembl
chr6:33504436..33510371hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385936
hg195936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411308
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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