A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391401



Internal ID21048954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176867804..176868405hg38UCSC Ensembl
chr4:177788958..177789559hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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