A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358731



Internal ID21016284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30380901..30384700hg38UCSC Ensembl
chr4:30382523..30386322hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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