A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753615



Internal ID21387439
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 StatusS
Merged Variantsnsv4434251
Supporting Variants
SamplesMDQ045
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753615
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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