A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357202



Internal ID21014755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29514753..29515207hg38UCSC Ensembl
chr4:29516375..29516829hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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