A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602589



Internal ID20975660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167113608..167115246hg38UCSC Ensembl
chr6:167527096..167528734hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381639
hg191639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140512
Samples
Known GenesCCR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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