A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798733



Internal ID21244071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34132665..34132840hg38UCSC Ensembl
chr19:34623570..34623745hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798733
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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