A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813268



Internal ID21258606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106859931..106860118hg38UCSC Ensembl
chr8:105231728..105231869hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38188
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711538
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813268
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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