A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592346



Internal ID20965417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122384682..122385391hg38UCSC Ensembl
chr10:124144198..124144907hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv906n223
Supporting Variantsnssv18234383
Samples
Known GenesPLEKHA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592346
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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