A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682592



Internal ID21204449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:121744..121744hg38UCSC Ensembl
chr3:197891187..197891187hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796478
Supporting Variants
Samples
Known GenesFAM157A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682592
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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