A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789607



Internal ID21234945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23111787..23111840hg38UCSC Ensembl
chr10:23400716..23400769hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699639
Samples
Known GenesMSRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789607
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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