A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330309



Internal ID20863465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219087506..219404470hg38UCSC Ensembl
chr1:219260848..219577812hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38316965
hg19316965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058107
Samples
Known GenesLOC643723, LYPLAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330309
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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