A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611272



Internal ID20984343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98408920..98440510hg38UCSC Ensembl
chr7:98038232..98069822hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3831591
hg1931591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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