A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446395



Internal ID22112574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76602139..76602139hg38UCSC Ensembl
chr11:76313183..76313183hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768239
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446395
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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