A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862230



Internal ID22637165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48859268..48860792hg38UCSC Ensembl
chr12:49253051..49254575hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381525
hg191525
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453231
Samples
Known GenesRND1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862230
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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