A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437021



Internal ID22103198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117097427..117097427hg38UCSC Ensembl
chr8:118109666..118109666hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760556
Samples
Known GenesSLC30A8
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437021
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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