A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688437



Internal ID21210291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15350238..15350238hg38UCSC Ensembl
chr4:15351862..15351862hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810309
Supporting Variants
Samples
Known GenesC1QTNF7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688437
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.617647


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