A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803167



Internal ID21248505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54131500..54131500hg38UCSC Ensembl
chr20:52748039..52748039hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803167
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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