A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330290



Internal ID20863446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223991905..223992699hg38UCSC Ensembl
chr1:224179607..224180401hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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