A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017144



Internal ID21926487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73457282..73457425hg38UCSC Ensembl
chr7:72871612..72871755hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577192
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017144
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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