A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039028



Internal ID21948371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34315037..34333448hg38UCSC Ensembl
chr18:31895001..31913412hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3818412
hg1918412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039028
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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