A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572083



Internal ID20945154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65893263..65894248hg38UCSC Ensembl
chr7:65358250..65359235hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274249
Samples
Known GenesVKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572083
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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