A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404980



Internal ID21062533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56391246..56425967hg38UCSC Ensembl
chr6:56256044..56290765hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3834722
hg1934722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146537
Samples
Known GenesRNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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