A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400005



Internal ID21057558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10107441..10146869hg38UCSC Ensembl
chr6:10107674..10147102hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3839429
hg1939429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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