A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579693



Internal ID20952764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73178211..73179031hg38UCSC Ensembl
chr10:74937969..74938789hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv806n223
Supporting Variantsnssv18231592
Samples
Known GenesFAM149B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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