A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579684



Internal ID20952755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68134740..68135126hg38UCSC Ensembl
chr10:69894497..69894883hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218663
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579684
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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