A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039316



Internal ID21948659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35168812..35168874hg38UCSC Ensembl
chr18:32748776..32748838hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039316
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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