A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418268



Internal ID21075821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56552356..56557874hg38UCSC Ensembl
chr8:57464915..57470433hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385519
hg195519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169205
Samples
Known GenesLINC00968
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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