A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857309



Internal ID22632244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14934983..14938319hg38UCSC Ensembl
chr12:15087917..15091253hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463649
Samples
Known GenesERP27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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