A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326047



Internal ID20859181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:196651851..196652423hg38UCSC Ensembl
chr1:196620981..196621553hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055659
Samples
Known GenesCFH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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