A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101804



Internal ID22011037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72732292..72732292hg38UCSC Ensembl
chr18:70399527..70399527hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101804
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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