A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442462



Internal ID22108645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55266346..55266346hg38UCSC Ensembl
chr19:55777714..55777714hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767815
Samples
Known GenesHSPBP1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442462
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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