A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137265



Internal ID20704305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117800136..117853118hg38UCSC Ensembl
chr6:118121299..118174281hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3852983
hg1952983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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