A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250599



Internal ID20817639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63529612..63529802hg38UCSC Ensembl
chr1:63995283..63995473hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542032
Supporting Variants
Samples
Known GenesEFCAB7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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