A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757311



Internal ID20533171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30249101..30348816hg38UCSC Ensembl
chr12:30402034..30501749hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3899716
hg1999716
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv23n199
Supporting Variantsnssv16262086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757311
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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