A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801267



Internal ID21246605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206123453..206123453hg38UCSC Ensembl
chr1:206217878..206217878hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801267
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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