A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001596



Internal ID21910939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149280101..149280153hg38UCSC Ensembl
chr7:148977192..148977244hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570918
Samples
Known GenesZNF783
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001596
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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