A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805229



Internal ID21250567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16089997..16090092hg38UCSC Ensembl
chr2:16230119..16230214hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805229
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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