A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059665



Internal ID20626705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244713200..244720738hg38UCSC Ensembl
chr1:244876502..244884040hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg387539
hg197539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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