A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv712n172



Internal ID22815086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111319992..111321960hg38UCSC Ensembl
chr6:111641195..111643163hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381969
hg191969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434726, nsv4434725
SamplesMDQ045, BTQ038, BTQ016
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv712n172
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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