A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801384



Internal ID21246722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219411128..219411246hg38UCSC Ensembl
chr1:219584470..219584588hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801384
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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