A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7188n223



Internal ID22810156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152845501..153158224hg38UCSC Ensembl
chr7:152542586..152855309hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38312724
hg19312724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6415953, nsv6424471
Samples
Known GenesACTR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7188n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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