A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594748



Internal ID20967819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14972012..15457502hg38UCSC Ensembl
chr16:15065869..15551359hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38485491
hg19485491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2699n223
Supporting Variantsnssv18239958
Samples
Known GenesC16orf45, MIR3180-4, MIR6511B-1, MPV17L, NPIPA5, NTAN1, PDXDC1, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594748
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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