A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677355



Internal ID21199207
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 StatusS
Merged Variantsnsv2789641
Supporting Variants
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677355
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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