A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550481



Internal ID20923622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:130166764..131507183hg38UCSC Ensembl
chr2:130924337..132264756hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg381340420
hg191340420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4105n223
Supporting Variantsnssv18255228
Samples
Known GenesAMER3, ARHGEF4, CCDC115, CFC1, CFC1B, CYP4F30P, CYP4F62P, FAM168B, FAR2P2, GPR148, IMP4, LINC01120, LOC150776, LOC401010, LOC440910, LOC646743, MIR4784, MZT2A, MZT2B, PLEKHB2, POTEE, POTEI, POTEJ, PTPN18, RNU6-81P, SMPD4, TISP43, TUBA3D, TUBA3E, WTH3DI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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