A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139997



Internal ID20707037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21606418..21608545hg38UCSC Ensembl
chr6:21606649..21608776hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382128
hg192128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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