A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224093



Internal ID20791133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9448188..9496202hg38UCSC Ensembl
chr7:9487818..9535832hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3848015
hg1948015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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