A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410217



Internal ID21067770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87641331..87642102hg38UCSC Ensembl
chr6:88351049..88351820hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224486
Samples
Known GenesORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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