A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577107



Internal ID20950178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16594894..16595743hg38UCSC Ensembl
chr10:16636893..16637742hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231948
Samples
Known GenesRSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577107
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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