A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441922



Internal ID22108104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43780537..43780537hg38UCSC Ensembl
chr19:44284689..44284689hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757695
Samples
Known GenesKCNN4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441922
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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