A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443971



Internal ID22110152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59442200..59442200hg38UCSC Ensembl
chr20:58017255..58017255hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757700
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443971
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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