A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413417



Internal ID21070970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95666601..95674000hg38UCSC Ensembl
chr6:96114477..96121876hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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