A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv699n172



Internal ID22815073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51589865..51610903hg38UCSC Ensembl
chr6:51454663..51475701hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3821039
hg1921039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434984, nsv4434985
SamplesMDQ010, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv699n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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