A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232598



Internal ID20799638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69136960..69212906hg38UCSC Ensembl
chr6:69846852..69922798hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3875947
hg1975947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397943
Supporting Variants
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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