A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373469



Internal ID21031022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8222987..8431104hg38UCSC Ensembl
chr4:8224714..8432831hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38208118
hg19208118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119886
Samples
Known GenesACOX3, HTRA3, SH3TC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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