A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605213



Internal ID20978284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84552156..84749219hg38UCSC Ensembl
chr7:84181472..84378535hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38197064
hg19197064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161048
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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