A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595307



Internal ID20968378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1516512..2069676hg38UCSC Ensembl
chr16:1566513..2119677hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38553165
hg19553165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238470
Samples
Known GenesCRAMP1L, EME2, FAHD1, GFER, HAGH, HN1L, HS3ST6, IFT140, IGFALS, LINC00254, MAPK8IP3, MEIOB, MIR3177, MRPS34, MSRB1, NDUFB10, NME3, NOXO1, NPW, NTHL1, NUBP2, RNF151, RPL3L, RPS2, SLC9A3R2, SNHG9, SNORA10, SNORA64, SNORA78, SPSB3, SYNGR3, TBL3, TMEM204, TSC2, ZNF598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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