A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584124



Internal ID20957195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21583121..22699430hg38UCSC Ensembl
chr16:21594442..22710751hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381116310
hg191116310
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2728n223
Supporting Variantsnssv18239255
Samples
Known GenesC16orf52, CDR2, EEF2K, IGSF6, LOC653786, METTL9, NPIPB5, OTOA, PDZD9, POLR3E, RRN3P1, RRN3P3, SMG1P1, UQCRC2, VWA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584124
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer