A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424447



Internal ID21082000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10346684..10384062hg38UCSC Ensembl
chr8:10204194..10241572hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3837379
hg1937379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162626
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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