A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576763



Internal ID20949834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81262059..82043442hg38UCSC Ensembl
chr16:81295664..82077047hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38781384
hg19781384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240194
Samples
Known GenesBCMO1, CMIP, GAN, HSD17B2, LOC100129617, MIR4720, MIR6504, MIR7854, PLCG2, SDR42E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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