A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417461



Internal ID21075014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155112609..155166498hg38UCSC Ensembl
chr7:154904319..154958208hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3853890
hg1953890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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