A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110397



Internal ID20677437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156957012..156959357hg38UCSC Ensembl
chr4:157878164..157880509hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392330
Supporting Variants
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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