A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593480



Internal ID20966551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2733607..2740823hg38UCSC Ensembl
chr16:2783608..2790824hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387217
hg197217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242808
Samples
Known GenesSRRM2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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