A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605758



Internal ID20978829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80234314..80300215hg38UCSC Ensembl
chr7:79863630..79929531hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3865902
hg1965902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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