A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548406



Internal ID20921592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157016528..157017724hg38UCSC Ensembl
chr1:156986320..156987516hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247756
Samples
Known GenesARHGEF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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