A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186024



Internal ID21324839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939008..2939008hg38UCSC Ensembl
chr19:2939006..2939006hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951363
Supporting Variants
SamplesHG002
Known GenesZNF77
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186024
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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