A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564403



Internal ID20937474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29963174..29969549hg38UCSC Ensembl
chr7:30002790..30009165hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg386376
hg196376
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273454
Samples
Known GenesSCRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564403
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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