A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868662



Internal ID22643597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:106240685..107908171hg38UCSC Ensembl
chr2:106857141..108524627hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg381667487
hg191667487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402388
Samples
Known GenesPLGLA, RGPD3, RGPD4, RGPD4-AS1, ST6GAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868662
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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