A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv740n172



Internal ID22815114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170266527..170267735hg38UCSC Ensembl
chr6:170575615..170576823hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434867, nsv4434872, nsv4434868, nsv4434871, nsv4434870, nsv4434869
SamplesMDQ045, BTQ038, BTQ055, NB11, NB07, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv740n172
Frequency
Sample Size15
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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