A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137774



Internal ID20704814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128744037..128747903hg38UCSC Ensembl
chr6:129065182..129069048hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg383867
hg193867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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