A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852487



Internal ID22627422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121966687..121968834hg38UCSC Ensembl
chr12:122404593..122406740hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462255
Samples
Known GenesWDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852487
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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