A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591843



Internal ID20964914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4398736..4642752hg38UCSC Ensembl
chr16:4448737..4692753hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38244017
hg19244017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240636
Samples
Known GenesC16orf96, CDIP1, CORO7, CORO7-PAM16, DNAJA3, HMOX2, MGRN1, NMRAL1, UBALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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