A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445496



Internal ID22111675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19859957..19859957hg38UCSC Ensembl
chr11:19881503..19881503hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761209
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445496
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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