A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547221



Internal ID20920426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42505374..42506067hg38UCSC Ensembl
chr2:42732514..42733207hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257935
Samples
Known GenesMTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547221
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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