A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421346



Internal ID21078899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8790982..8792407hg38UCSC Ensembl
chr8:8648492..8649917hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381426
hg191426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171024
Samples
Known GenesMFHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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