A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560328



Internal ID20933399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38071889..38073642hg38UCSC Ensembl
chr7:38111491..38113244hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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