A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790704



Internal ID21236042
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 StatusM
Merged Variants
Supporting Variantsnssv13698647
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790704
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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