A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1151n145



Internal ID22814167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155295188..155299929hg38UCSC Ensembl
chr7:155086898..155091639hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384742
hg194742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110999, nsv3110346
Samplessample93, sample208
Known GenesINSIG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1151n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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