A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813358



Internal ID21258696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3402418..3402418hg38UCSC Ensembl
chr6:3402652..3402652hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697205
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813358
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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