A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525126



Internal ID20898487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38656553..38656976hg38UCSC Ensembl
chr18:36236517..36236940hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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