A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438567



Internal ID22104747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28813598..28813598hg38UCSC Ensembl
chr10:29102527..29102527hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757971
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438567
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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