A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565602



Internal ID20938673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125128997..125129633hg38UCSC Ensembl
chr9:127891276..127891912hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279861
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565602
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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