A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360963



Internal ID21018516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29396303..29396810hg38UCSC Ensembl
chr4:29397925..29398432hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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