A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375670



Internal ID21033223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40411110..40411498hg38UCSC Ensembl
chr5:40411212..40411600hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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