A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102137



Internal ID22011371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29521410..29521410hg38UCSC Ensembl
chr18:27101375..27101375hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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