A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707150



Internal ID21228944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130221890..130221890hg38UCSC Ensembl
chr9:132984169..132984169hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818266
Supporting Variants
Samples
Known GenesNCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707150
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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