A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860156



Internal ID22635091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75296019..75298076hg38UCSC Ensembl
chr12:75689799..75691856hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469067, nssv17466281
Samples
Known GenesCAPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860156
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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