A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360070



Internal ID21017623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1155092..1160329hg38UCSC Ensembl
chr4:1148880..1154117hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg385238
hg195238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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