A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6857n223



Internal ID22809825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64029689..64357899hg38UCSC Ensembl
chr7:63490067..63818277hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38328211
hg19328211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6607450, nsv6618015, nsv6615819
Samples
Known GenesLINC01005, ZNF679, ZNF727, ZNF735, ZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6857n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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