A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315799



Internal ID20848873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185279294..185285311hg38UCSC Ensembl
chr1:185248426..185254443hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054475
Samples
Known GenesSWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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