A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053924



Internal ID20620964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17259698..17267500hg38UCSC Ensembl
chr1:17586193..17593995hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg387803
hg197803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321333
Supporting Variants
Samples
Known GenesPADI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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