A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571678



Internal ID20944749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76420466..76420750hg38UCSC Ensembl
chr9:79035382..79035666hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571678
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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