A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143128



Internal ID20710168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19289472..19292069hg38UCSC Ensembl
chr6:19289703..19292300hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382598
hg192598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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