A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609135



Internal ID20982206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79937423..79961606hg38UCSC Ensembl
chr7:79566739..79590922hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3824184
hg1924184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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