A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854324



Internal ID22629259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5846528..5849560hg38UCSC Ensembl
chr12:5955694..5958726hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383033
hg193033
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463613
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854324
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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