A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702353



Internal ID21224188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136074453..136074453hg38UCSC Ensembl
chr9:138966299..138966299hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819517
Supporting Variants
Samples
Known GenesNACC2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702353
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.884615


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