A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767813



Internal ID22102287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53819411..53819411hg38UCSC Ensembl
chr19:54322665..54322665hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4442122
Supporting Variants
Samples
Known GenesNLRP12
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767813
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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