A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382505



Internal ID21040058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141809449..141886917hg38UCSC Ensembl
chr4:142730602..142808070hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3877469
hg1977469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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