A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607117



Internal ID20980188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114067327..114068273hg38UCSC Ensembl
chr6:114388491..114389437hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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