A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619173



Internal ID20992244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80984317..80987532hg38UCSC Ensembl
chr7:80613633..80616848hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg383216
hg193216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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