A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101830



Internal ID22011063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53895136..53895136hg38UCSC Ensembl
chr18:51421506..51421506hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101830
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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