A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570469



Internal ID20943540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45523570..45523874hg38UCSC Ensembl
chr6:45491307..45491611hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271980
Samples
Known GenesRUNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570469
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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