A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743531



Internal ID20519519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1185462..1185998hg38UCSC Ensembl
chr4:1179250..1179786hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274467
Samples
Known GenesSPON2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743531
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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