A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553935



Internal ID20927045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:744578..1222235hg38UCSC Ensembl
chr2:744578..1218595hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38477658
hg19474018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258364
Samples
Known GenesLINC01115, SNTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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