A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333959



Internal ID20867140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160993642..160996937hg38UCSC Ensembl
chr1:160963432..160966727hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052486
Samples
Known GenesF11R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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