A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805303



Internal ID21250641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112732317..112732317hg38UCSC Ensembl
chr2:113489894..113489894hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805303
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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