A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142771



Internal ID20709811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49180623..49181173hg38UCSC Ensembl
chr6:49148259..49148809hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00084


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