A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544668



Internal ID20917905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:50390446..50450433hg38UCSC Ensembl
chr2:50617584..50677571hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3859988
hg1959988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258723
Samples
Known GenesNRXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544668
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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