A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831312



Internal ID22606247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135340753..135344036hg38UCSC Ensembl
chr2:136098323..136101606hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487293
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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