A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6557n223



Internal ID22809525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6793901..7334700hg38UCSC Ensembl
chr7:6833532..7374331hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38540800
hg19540800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6616738, nsv6608388, nsv6610960, nsv6619857
Samples
Known GenesC1GALT1, CCZ1B, LOC100131257, LOC101927354, RSPH10B, RSPH10B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6557n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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