A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6610n223



Internal ID22809578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18166201..18350900hg38UCSC Ensembl
chr7:18205824..18390523hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38184700
hg19184700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6606923, nsv6602243
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6610n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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