A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051159



Internal ID20618199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10936458..10944977hg38UCSC Ensembl
chr1:10996515..11005034hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg388520
hg198520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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