A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869255



Internal ID22644190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:196798831..196923676hg38UCSC Ensembl
chr1:196767961..196892806hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38124846
hg19124846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv114n209
Supporting Variantsnssv17361060
Samples
Known GenesCFHR1, CFHR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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