A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602647



Internal ID20975718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137006710..137011799hg38UCSC Ensembl
chr6:137327847..137332936hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385090
hg195090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138319
Samples
Known GenesIL20RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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