A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6562n223



Internal ID22809530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6823601..7116300hg38UCSC Ensembl
chr7:6863232..7155931hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38292700
hg19292700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6602636, nsv6616973
Samples
Known GenesCCZ1B, LOC100131257
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6562n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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