A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383226



Internal ID21040779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103404908..103405330hg38UCSC Ensembl
chr4:104326065..104326487hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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