A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952507



Internal ID21372576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33953227..33953227hg38UCSC Ensembl
chr18:31533191..31533191hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185944
SamplesHG002
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952507
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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