A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575102



Internal ID20948173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26212247..26213321hg38UCSC Ensembl
chr9:26212245..26213319hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7663n223
Supporting Variantsnssv18280392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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