A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235865



Internal ID20802905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80835767..80848532hg38UCSC Ensembl
chr7:80465083..80477848hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3812766
hg1912766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605782
Supporting Variants
Samples
Known GenesSEMA3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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