A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145300



Internal ID20712340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82867830..82871070hg38UCSC Ensembl
chr6:83577549..83580789hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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