A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058553



Internal ID20625593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229693871..229695412hg38UCSC Ensembl
chr1:229829618..229831159hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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