A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571435



Internal ID20944506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9267910..9307376hg38UCSC Ensembl
chr7:9307540..9347006hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3839467
hg1939467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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