A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000752



Internal ID21910095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129932274..129932345hg38UCSC Ensembl
chr7:129572114..129572185hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561687
Samples
Known GenesUBE2H
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000752
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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