A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235155



Internal ID20802195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56093026..56101971hg38UCSC Ensembl
chr8:57005585..57014530hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg388946
hg198946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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