A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796566



Internal ID21241904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1035592..1035592hg38UCSC Ensembl
chr17:938832..938832hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691961
Samples
Known GenesABR
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796566
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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