A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068381



Internal ID21490726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119287037..119292120hg38UCSC Ensembl
chr10:121046549..121051632hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg385084
hg195084
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672348
Supporting Variants
SamplesNA19238
Known GenesGRK5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068381
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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