A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389734



Internal ID21047287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41994992..41997564hg38UCSC Ensembl
chr4:41997009..41999581hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382573
hg192573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116393
Samples
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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