A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679637



Internal ID21201499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93876122..93876122hg38UCSC Ensembl
chr1:94341678..94341678hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382504
hg192504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802354
Supporting Variants
Samples
Known GenesDNTTIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679637
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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