A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801883



Internal ID21247221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47592604..47592604hg38UCSC Ensembl
chr1:48058276..48058276hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801883
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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