A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671055



Internal ID21619360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112180273..112235875hg38UCSC Ensembl
chr5:111515970..111571572hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3855603
hg1955603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126206
SamplesNA18534
Known GenesEPB41L4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671055
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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