A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413927



Internal ID21071480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87349044..87386027hg38UCSC Ensembl
chr6:88058762..88095745hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3836984
hg1936984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228330
Samples
Known GenesC6orf163
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413927
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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