A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404385



Internal ID21061938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3942807..3944546hg38UCSC Ensembl
chr6:3943041..3944780hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381740
hg191740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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