A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442387



Internal ID22108570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165678007..165678007hg38UCSC Ensembl
chr6:166091495..166091495hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756231
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442387
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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