A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411577



Internal ID21069130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43412501..43414100hg38UCSC Ensembl
chr6:43380239..43381838hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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