A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321023



Internal ID20854125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158140095..158143536hg38UCSC Ensembl
chr1:158109885..158113326hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg383442
hg193442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052743
Samples
Known GenesLOC646268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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