A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587750



Internal ID20960821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122384628..122385335hg38UCSC Ensembl
chr10:124144144..124144851hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv906n223
Supporting Variantsnssv18223426
Samples
Known GenesPLEKHA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587750
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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