A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789699



Internal ID21235037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102601117..102601432hg38UCSC Ensembl
chr11:102471848..102472163hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688226
Samples
Known GenesMMP20
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789699
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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