A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608771



Internal ID20981842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123188520..124009575hg38UCSC Ensembl
chr6:123509665..124330720hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38821056
hg19821056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214597
Samples
Known GenesNKAIN2, TRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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