A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6573n223



Internal ID22809541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8800291..8931216hg38UCSC Ensembl
chr7:8839921..8970846hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38130926
hg19130926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6615937, nsv6611832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6573n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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