A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980234



Internal ID22755169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:130052690..131284721hg38UCSC Ensembl
chr2:130810263..132042294hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg381232032
hg191232032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1232n209
Supporting Variantsnssv17391484
Samples
Known GenesAMER3, ARHGEF4, CCDC115, CCDC74B, CFC1, CFC1B, CYP4F30P, CYP4F62P, FAM168B, FAR2P2, GPR148, IMP4, LOC440910, LOC646743, MED15P9, MZT2B, PLEKHB2, POTEE, POTEF, POTEI, POTEJ, PTPN18, SMPD4, TISP43, TUBA3E
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980234
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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