A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061564



Internal ID20628604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46499181..46501352hg38UCSC Ensembl
chr1:46964853..46967024hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg382172
hg192172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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