A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808554



Internal ID21253892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16393061..16393182hg38UCSC Ensembl
chr4:16394684..16394805hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808554
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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