A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257751



Internal ID21398429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50132877..50360806hg38UCSC Ensembl
chr11:50092048..50319977hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38227930
hg19227930
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730168
Supporting Variants
SamplesHG00513
Known GenesLOC441601
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257751
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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