A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234441



Internal ID20801481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97761901..97779100hg38UCSC Ensembl
chr7:97391213..97408412hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3817200
hg1917200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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