A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330124



Internal ID20863278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88938522..88944400hg38UCSC Ensembl
chr1:89404205..89410083hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385879
hg195879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064898
Samples
Known GenesCCBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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