A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv725n172



Internal ID22815099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159665082..159667790hg38UCSC Ensembl
chr6:160086114..160088822hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382709
hg192709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434801, nsv4434802, nsv4434805, nsv4434804, nsv4434803
SamplesMDQ045, BTQ055, MDQ010, SMI041, NB11, NB07, SMI018, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv725n172
Frequency
Sample Size15
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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