A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034578



Internal ID21943921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61790672..61803641hg38UCSC Ensembl
chr18:59457905..59470874hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3812970
hg1912970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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