A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232317



Internal ID20799357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92698916..92718602hg38UCSC Ensembl
chr6:93408634..93428320hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3819687
hg1919687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232317
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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