A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684203



Internal ID21206059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232725423..232725423hg38UCSC Ensembl
chr1:232861169..232861169hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684203
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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