A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376681



Internal ID21034234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40093015..40094063hg38UCSC Ensembl
chr5:40093117..40094165hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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