A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614883



Internal ID20987954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169749201..169754100hg38UCSC Ensembl
chr6:170149297..170154196hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216148
Samples
Known GenesERMARD, TCTE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614883
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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