A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552709



Internal ID20925835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55247293..55248037hg38UCSC Ensembl
chr2:55474429..55475173hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258218
Samples
Known GenesMTIF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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