A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814861



Internal ID21260199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28382865..28382950hg38UCSC Ensembl
chr6:28350642..28350727hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696610
Samples
Known GenesZSCAN12
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814861
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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