A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058027



Internal ID20625067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221492076..221493538hg38UCSC Ensembl
chr1:221665418..221666880hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381463
hg191463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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