A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7162n223



Internal ID22810130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146527528..147051293hg38UCSC Ensembl
chr7:146224620..146748385hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38523766
hg19523766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6427062, nsv6435227
Samples
Known GenesCNTNAP2, MIR548AQ, MIR548AR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7162n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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