A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608968



Internal ID20982039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151189361..151208813hg38UCSC Ensembl
chr6:151510496..151529948hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3819453
hg1919453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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