A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552894



Internal ID20926015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:48367847..48368663hg38UCSC Ensembl
chr2:48594986..48595802hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258091
Samples
Known GenesFOXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552894
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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