A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536332



Internal ID20909681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85222648..85223136hg38UCSC Ensembl
chr2:85449771..85450259hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260902
Samples
Known GenesTCF7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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