A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606596



Internal ID20979667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143547671..143555567hg38UCSC Ensembl
chr6:143868808..143876704hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387897
hg197897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140239
Samples
Known GenesLOC285740
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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