A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434251



Internal ID21396253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168804092..168822088hg38UCSC Ensembl
chr4:169725243..169743239hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3817997
hg1917997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753615
SamplesMDQ045
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434251
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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