A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813066



Internal ID21258404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119798319..119798389hg38UCSC Ensembl
chr6:120119465..120119535hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813066
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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