A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228577



Internal ID20795617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13866735..13867290hg38UCSC Ensembl
chr10:13908735..13909290hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579341
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228577
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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