A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186195



Internal ID21325019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49169391..49169391hg38UCSC Ensembl
chr19:49672648..49672648hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382757
hg192757
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939163
Supporting Variants
SamplesHG002
Known GenesTRPM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186195
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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