A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807448



Internal ID21252787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2905249..2905338hg38UCSC Ensembl
chr2:2909021..2909110hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807448
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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