A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422436



Internal ID21079989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149474301..149476400hg38UCSC Ensembl
chr7:149171392..149173491hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224457
Samples
Known GenesZNF746
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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