A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789641



Internal ID21234979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3085781..3085781hg38UCSC Ensembl
chr10:3127973..3127973hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677355
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789641
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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