A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232752



Internal ID20799792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137981415..137995194hg38UCSC Ensembl
chr8:138993658..139007437hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3813780
hg1913780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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