A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409266



Internal ID21066819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87613420..87615335hg38UCSC Ensembl
chr6:88323138..88325053hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381916
hg191916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222985
Samples
Known GenesORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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