A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330841



Internal ID20863999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157027955..157033901hg38UCSC Ensembl
chr1:156997747..157003693hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg385947
hg195947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052295
Samples
Known GenesARHGEF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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