A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333898



Internal ID20867079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21762760..21763700hg38UCSC Ensembl
chr1:22089253..22090193hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057622
Samples
Known GenesUSP48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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