A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364672



Internal ID21022225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27923587..27924002hg38UCSC Ensembl
chr4:27925209..27925624hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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