A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331009



Internal ID20864169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28430159..28433520hg38UCSC Ensembl
chr1:28756670..28760031hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383362
hg193362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059939
Samples
Known GenesPHACTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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