A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788822



Internal ID21234160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133203094..133203201hg38UCSC Ensembl
chr10:135016598..135016705hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683821
Samples
Known GenesKNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788822
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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