A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383181



Internal ID21040734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129770201..129771000hg38UCSC Ensembl
chr4:130691356..130692155hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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