A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214156



Internal ID20781196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78380401..78393700hg38UCSC Ensembl
chr5:77676225..77689524hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3813300
hg1913300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403095
Supporting Variants
Samples
Known GenesSCAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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