A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445684



Internal ID22111861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412717..32412717hg38UCSC Ensembl
chr11:32434263..32434263hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757386
Samples
Known GenesWT1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445684
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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