A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201614



Internal ID21340413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174114282..174114282hg38UCSC Ensembl
chr5:173541285..173541285hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939351
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201614
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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