A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790680



Internal ID21236018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61867911..61868044hg38UCSC Ensembl
chr11:61635383..61635516hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790680
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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