A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216730



Internal ID20783770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160490775..160496292hg38UCSC Ensembl
chr6:160911807..160917324hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385518
hg195518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606925
Supporting Variants
Samples
Known GenesLPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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