A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv673n172



Internal ID22815047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3618911..3621639hg38UCSC Ensembl
chr6:3619145..3621873hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434963, nsv4434964
SamplesBTQ038, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv673n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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