A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065688



Internal ID21512750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60775308..60780330hg38UCSC Ensembl
chr1:61240980..61246002hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg385023
hg195023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669854
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065688
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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