A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381229



Internal ID21038782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151965554..151966521hg38UCSC Ensembl
chr4:152886706..152887673hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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