A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv722n172



Internal ID22815096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157278769..157283338hg38UCSC Ensembl
chr6:157699801..157704370hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384570
hg194570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434796, nsv4434795, nsv4434792, nsv4434791, nsv4434793, nsv4434794
SamplesNB08, MDQ045, BTQ038, BTQ055, MDQ010, BTQ016, SMI041, NB11, SMI018, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv722n172
Frequency
Sample Size15
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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