A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385364



Internal ID21042917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69742608..69743773hg38UCSC Ensembl
chr4:70608326..70609491hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119026
Samples
Known GenesSULT1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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