A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143306



Internal ID20710346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40942476..40944494hg38UCSC Ensembl
chr6:40910215..40912233hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382019
hg192019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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