A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668005



Internal ID21616312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155308355..155353241hg38UCSC Ensembl
chr7:155100065..155145941hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3844887
hg1945877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143824
Samples
Known GenesINSIG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668005
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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