A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806536



Internal ID21251874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60418464..60418464hg38UCSC Ensembl
chr2:60645599..60645599hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806536
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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