A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801259



Internal ID21246599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202205247..202205247hg38UCSC Ensembl
chr1:202174375..202174375hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683484
Samples
Known GenesLGR6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801259
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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