A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700772



Internal ID21222613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27749221..27749221hg38UCSC Ensembl
chr2:27972088..27972088hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700772
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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