A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218783



Internal ID20785823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46956065..47010614hg38UCSC Ensembl
chr7:46995663..47050212hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3854550
hg1954550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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