A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552761



Internal ID20925887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37748378..37749108hg38UCSC Ensembl
chr1:38214050..38214780hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251076
Samples
Known GenesEPHA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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