A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333389



Internal ID20866565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161265736..161271141hg38UCSC Ensembl
chr1:161235526..161240931hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg385406
hg195406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053250
Samples
Known GenesPCP4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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