A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138353



Internal ID20705393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13768501..13770300hg38UCSC Ensembl
chr6:13768733..13770532hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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