A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325667



Internal ID20858798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165910969..165912206hg38UCSC Ensembl
chr1:165880206..165881443hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052850
Samples
Known GenesUCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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