A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557854



Internal ID20930925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65941699..65942495hg38UCSC Ensembl
chr7:65406686..65407482hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274256
Samples
Known GenesVKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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