A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678854



Internal ID21200714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181078275..181078275hg38UCSC Ensembl
chr1:181047411..181047411hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678854
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.46875


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