A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756737



Internal ID20532597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21583120..22699429hg38UCSC Ensembl
chr16:21594441..22710750hg19UCSC 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 Variants
Supporting Variantsnssv16268081
Samples
Known GenesC16orf52, CDR2, EEF2K, IGSF6, LOC653786, METTL9, NPIPB5, OTOA, PDZD9, POLR3E, RRN3P1, RRN3P3, SMG1P1, UQCRC2, VWA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756737
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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