A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054716



Internal ID20621756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183613401..183619000hg38UCSC Ensembl
chr1:183582536..183588135hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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