A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035774



Internal ID21945117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44533479..44535392hg38UCSC Ensembl
chr18:42113444..42115357hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381914
hg191914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035774
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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