A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536393



Internal ID20909741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:131595934..133010486hg38UCSC Ensembl
chr2:132353507..133768059hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg381414553
hg191414553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255246
Samples
Known GenesANKRD30BL, C2orf27A, C2orf27B, GPR39, LINC01087, LYPD1, MIR663B, MIR7853, NCKAP5, POTEKP, RNU6-81P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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