A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805837



Internal ID21251175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17753325..17753325hg38UCSC Ensembl
chr2:17934592..17934592hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683763
Samples
Known GenesSMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805837
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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