A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145938



Internal ID20712978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83929692..83930192hg38UCSC Ensembl
chr6:84639411..84639911hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414117
Supporting Variants
Samples
Known GenesCYB5R4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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