A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698647



Internal ID21220497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68415627..68415936hg38UCSC Ensembl
chr11:68183095..68183404hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790704
Supporting Variants
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698647
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.765625


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