A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548377



Internal ID20921564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:130018897..131305573hg38UCSC Ensembl
chr2:130776470..132063146hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg381286677
hg191286677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4105n223
Supporting Variantsnssv18255221
Samples
Known GenesAMER3, ARHGEF4, CCDC115, CCDC74B, CFC1, CFC1B, CYP4F30P, CYP4F62P, FAM168B, FAR2P1, FAR2P2, GPR148, IMP4, LOC440910, LOC646743, MED15P9, MZT2B, PLEKHB2, POTEE, POTEF, POTEI, POTEJ, PTPN18, SMPD4, TISP43, TUBA3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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