A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325019



Internal ID20858149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28242578..28245235hg38UCSC Ensembl
chr1:28569089..28571746hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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