A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521313



Internal ID20894674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76602028..76748383hg38UCSC Ensembl
chr18:74313985..74460339hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38146356
hg19146355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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