A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421942



Internal ID21079495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145781001..145790200hg38UCSC Ensembl
chr7:145478094..145487293hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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