A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441923



Internal ID22108105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43798137..43798137hg38UCSC Ensembl
chr19:44302289..44302289hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760455
Samples
Known GenesLYPD5
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441923
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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