A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1118n145



Internal ID22814134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92446162..92448876hg38UCSC Ensembl
chr7:92075476..92078190hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg382715
hg192715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111258, nsv3116352
Samplessample141, sample348
Known GenesGATAD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1118n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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