A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577549



Internal ID20950620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50042762..50136693hg38UCSC Ensembl
chr10:51802522..51896453hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3893932
hg1993932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv737n223
Supporting Variantsnssv18233852
Samples
Known GenesFAM21A, FAM21B, FLJ31813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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