A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv367n137



Internal ID22812987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67538278..67538625hg38UCSC Ensembl
chr9:65906803..65907123hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38348
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2819700, nsv2819343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv367n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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