A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798114



Internal ID21243452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82081885..82081942hg38UCSC Ensembl
chr17:80039761..80039818hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678513
Samples
Known GenesFASN
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798114
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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