A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385796



Internal ID21043349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82648110..82658208hg38UCSC Ensembl
chr4:83569263..83579361hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3810099
hg1910099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119904
Samples
Known GenesSCD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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