A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603116



Internal ID20976187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2346422..2346703hg38UCSC Ensembl
chr7:2386057..2386338hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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