A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614874



Internal ID20987945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165279748..165286103hg38UCSC Ensembl
chr6:165693237..165699592hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386356
hg196356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142390
Samples
Known GenesC6orf118
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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