A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800839



Internal ID21246177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181426705..181426705hg38UCSC Ensembl
chr1:181395841..181395841hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800839
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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