A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378629



Internal ID21036182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118896130..118898946hg38UCSC Ensembl
chr4:119817285..119820101hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg382817
hg192817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108353
Samples
Known GenesSYNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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