A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703091



Internal ID21224906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130222007..130222007hg38UCSC Ensembl
chr9:132984286..132984286hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818267
Supporting Variants
Samples
Known GenesNCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703091
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.265625


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