A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323388



Internal ID20856506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91041068..91046868hg38UCSC Ensembl
chr1:91506625..91512425hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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