A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439466



Internal ID22105644
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 Variantsnssv15767297
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439466
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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