A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135454



Internal ID20702495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112198072..112198581hg38UCSC Ensembl
chr6:112519274..112519783hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616842
Supporting Variants
Samples
Known GenesLAMA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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