A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6640n223



Internal ID22809608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35898791..35974554hg38UCSC Ensembl
chr7:35938401..36014164hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3875764
hg1975764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6620015, nsv6609538
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6640n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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