A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438920



Internal ID22105097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33128044..33128044hg38UCSC Ensembl
chr10:33416972..33416972hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759119
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438920
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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