A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332091



Internal ID20865260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173048001..173050700hg38UCSC Ensembl
chr1:173017141..173019840hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053961
Samples
Known GenesTNFSF18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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