A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414117



Internal ID21071670
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 StatusM
Merged Variants
Supporting Variantsnssv18145938
Samples
Known GenesCYB5R4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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