A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321540



Internal ID20854647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226256702..226260726hg38UCSC Ensembl
chr1:226444403..226448427hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058409
Samples
Known GenesLIN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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