A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763014



Internal ID20538874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:61079861..61204522hg38UCSC Ensembl
chr12:61473642..61598303hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38124662
hg19124662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763014
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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