A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161797



Internal ID20728837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93512049..93512473hg38UCSC Ensembl
chr7:93141361..93141785hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606858
Supporting Variants
Samples
Known GenesCALCR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00141


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