A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832825



Internal ID22607760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237886562..237887661hg38UCSC Ensembl
chr2:238795204..238796303hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483419, nssv17483418
Samples
Known GenesRAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832825
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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