A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692771



Internal ID21214621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50564279..50564279hg38UCSC Ensembl
chr1:51029951..51029951hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801973
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692771
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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