A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394469



Internal ID21052022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156897663..156898570hg38UCSC Ensembl
chr4:157818815..157819722hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110389
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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