A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051532



Internal ID20618572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13972947..13982028hg38UCSC Ensembl
chr1:14299442..14308523hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg389082
hg199082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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