A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850370



Internal ID22625305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121213129..121224083hg38UCSC Ensembl
chr12:121650932..121661886hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3810955
hg1910955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468256
Samples
Known GenesP2RX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850370
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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