A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290855



Internal ID20500073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30251015..30348809hg38UCSC Ensembl
chr12:30403948..30501742hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3897795
hg1997795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290855
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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