A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132731



Internal ID21512781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145693608..145694546hg38UCSC Ensembl
chr4:146614760..146615698hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668707
Supporting Variants
Samples
Known GenesC4orf51
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132731
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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