A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745901



Internal ID20521912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130042116..130045809hg38UCSC Ensembl
chr7:129681956..129685649hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg383694
hg193694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259596
Samples
Known GenesZC3HC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745901
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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