A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617162



Internal ID20990233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2323941..2343495hg38UCSC Ensembl
chr7:2363576..2383130hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3819555
hg1919555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617162
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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