A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328347



Internal ID20861494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182291536..182291985hg38UCSC Ensembl
chr1:182260671..182261120hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054667
Samples
Known GenesLOC400799
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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