A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324806



Internal ID20857935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28460651..28462438hg38UCSC Ensembl
chr1:28787162..28788949hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381788
hg191788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059945
Samples
Known GenesPHACTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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