A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616855



Internal ID20989926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79535457..79537746hg38UCSC Ensembl
chr7:79164773..79167062hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382290
hg192290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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