A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555199



Internal ID20928289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44649601..44690600hg38UCSC Ensembl
chr20:43278242..43319241hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3841000
hg1941000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202885
Samples
Known GenesADA, LOC79015
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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