A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420876



Internal ID21078429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152825449..152830714hg38UCSC Ensembl
chr7:152522534..152527799hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg385266
hg195266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156394
Samples
Known GenesACTR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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