A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737065



Internal ID20513022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149280079..149280131hg38UCSC Ensembl
chr7:148977170..148977222hg19UCSC 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 Variantsnssv16272667
Samples
Known GenesZNF783
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737065
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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