A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412857



Internal ID21070410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89841195..89843843hg38UCSC Ensembl
chr6:90550914..90553562hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145357
Samples
Known GenesCASP8AP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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