A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561790



Internal ID20934861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129981243..129981748hg38UCSC Ensembl
chr7:129621083..129621588hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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