A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575874



Internal ID20948945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7572913..7573590hg38UCSC Ensembl
chr10:7614876..7615553hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236867
Samples
Known GenesITIH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575874
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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