A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107451



Internal ID20674492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101049262..101049766hg38UCSC Ensembl
chr4:101970419..101970923hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392324
Supporting Variants
Samples
Known GenesPPP3CA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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