A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384435



Internal ID21041988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53203201..53215900hg38UCSC Ensembl
chr4:54069368..54082067hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5266n223
Supporting Variantsnssv18117397
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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