A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581431



Internal ID20954502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12131901..12132298hg38UCSC Ensembl
chr10:12173900..12174297hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236100
Samples
Known GenesSEC61A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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