A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130831



Internal ID21461826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177946130..178003952hg38UCSC Ensembl
chr5:177373131..177430953hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857823
hg1957823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665653
Supporting Variants
SamplesHG02818
Known GenesPROP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130831
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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