A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186870



Internal ID21325699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13936868..13936868hg38UCSC Ensembl
chr19:14047681..14047681hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951469
Supporting Variants
SamplesHG002
Known GenesPODNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186870
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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