A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138377



Internal ID20705417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138065712..138074411hg38UCSC Ensembl
chr6:138386849..138395548hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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