A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330119



Internal ID20863273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226533687..226547662hg38UCSC Ensembl
chr1:226721388..226735363hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3813976
hg1913976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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