A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736110



Internal ID20512055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42972878..42973004hg38UCSC Ensembl
chr4:42974895..42975021hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259601
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736110
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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