A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677283



Internal ID21199135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43183577..43183577hg38UCSC Ensembl
chr2:43410716..43410716hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677283
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.709677


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