A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807972



Internal ID21253310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309444..16309532hg38UCSC Ensembl
chr3:16350951..16351039hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807972
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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