A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556002



Internal ID20929073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105420866..105421605hg38UCSC Ensembl
chr9:108183147..108183886hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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