A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813055



Internal ID21258393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111903224..111908455hg38UCSC Ensembl
chr6:112224427..112229658hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385232
hg195232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813055
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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