A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691094



Internal ID21212951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202205285..202205285hg38UCSC Ensembl
chr1:202174413..202174413hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800966
Supporting Variants
Samples
Known GenesLGR6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691094
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5


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