A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559331



Internal ID20932402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128423511..128426374hg38UCSC Ensembl
chr7:128063565..128066428hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg382864
hg192864
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559331
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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