A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136886



Internal ID20703926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106744224..106744954hg38UCSC Ensembl
chr6:107192099..107192829hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609328
Supporting Variants
Samples
Known GenesLOC100422737
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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