A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379141



Internal ID21036694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156221894..156231803hg38UCSC Ensembl
chr4:157143046..157152955hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg389910
hg199910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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