A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201706



Internal ID21340510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9970738..9970738hg38UCSC Ensembl
chr5:9970850..9970850hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg383304
hg193304
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933067
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201706
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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