A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051064



Internal ID20618104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107519883..107522877hg38UCSC Ensembl
chr1:108062505..108065499hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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