A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061972



Internal ID20629012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51205713..51207295hg38UCSC Ensembl
chr1:51671385..51672967hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381583
hg191583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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