A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103515



Internal ID22012748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75767509..75767509hg38UCSC Ensembl
chr18:73479464..73479464hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103515
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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