A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv242n137



Internal ID22812862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171502855..171503113hg38UCSC Ensembl
chr3:171220644..171220902hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2806854, nsv2806855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv242n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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