A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335076



Internal ID20868267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165830024..165833700hg38UCSC Ensembl
chr1:165799261..165802937hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg383677
hg193677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052846
Samples
Known GenesUCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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