A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186151



Internal ID21324973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33760264..33760264hg38UCSC Ensembl
chr19:34251169..34251169hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947597
Supporting Variants
SamplesHG002
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186151
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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