A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322228



Internal ID20855339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39200570..39204145hg38UCSC Ensembl
chr1:39666242..39669817hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383576
hg193576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060097
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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