A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793945



Internal ID21239283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99408147..99408244hg38UCSC Ensembl
chr13:100060401..100060498hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793945
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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