A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201470



Internal ID21340270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39333608..39333608hg38UCSC Ensembl
chr5:39333710..39333710hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935527
Supporting Variants
SamplesHG002
Known GenesC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201470
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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