A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421241



Internal ID21078794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48653698..48662662hg38UCSC Ensembl
chr8:49566258..49575222hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg388965
hg198965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167753
Samples
Known GenesLOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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