A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516015



Internal ID20889376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28993295..29049973hg38UCSC Ensembl
chr18:26573259..26629937hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3856679
hg1956679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516015
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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