A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592431



Internal ID20965502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11672291..11672883hg38UCSC Ensembl
chr10:11714290..11714882hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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