A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556699



Internal ID20929770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83902711..85826507hg38UCSC Ensembl
chr9:86517626..88441422hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381923797
hg191923797
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281236
Samples
Known GenesAGTPBP1, C9orf64, HNRNPK, KIF27, LOC389765, MIR7-1, NTRK2, RMI1, SLC28A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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