A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571899



Internal ID20944970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156898820..156899661hg38UCSC Ensembl
chr4:157819972..157820813hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264863
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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