A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112288



Internal ID22021521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37157006..37157006hg38UCSC Ensembl
chr18:34736969..34736969hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619369
Samples
Known GenesKIAA1328
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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