A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669895



Internal ID21618200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97446411..97459144hg38UCSC Ensembl
chr7:97075723..97088456hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3812734
hg1912734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154260
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669895
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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