A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329238



Internal ID20862389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225547170..225552169hg38UCSC Ensembl
chr1:225734872..225739871hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058361
Samples
Known GenesENAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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