A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603960



Internal ID20977031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98519492..98534733hg38UCSC Ensembl
chr7:98148804..98164045hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3815242
hg1915242
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603960
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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