A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520651



Internal ID20894012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38575312..38576299hg38UCSC Ensembl
chr18:36155276..36156263hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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