A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589619



Internal ID20962690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50049509..50255036hg38UCSC Ensembl
chr10:51809269..52014796hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38205528
hg19205528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227992
Samples
Known GenesASAH2, FAM21A, FAM21B, FLJ31813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589619
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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