A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7169n223



Internal ID22810137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148973001..148979000hg38UCSC Ensembl
chr7:148670093..148676092hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6431952, nsv6423394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7169n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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