A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553311



Internal ID20926420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113382126..121687299hg38UCSC Ensembl
chr2:114139703..122444875hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg388305174
hg198305173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256534
Samples
Known GenesACTR3, C1QL2, C2orf76, CBWD2, CCDC93, CLASP1, DBI, DDX11L2, DDX18, DPP10, DPP10-AS1, EN1, EPB41L5, FAM138B, FOXD4L1, GLI2, INHBB, INSIG2, LINC01101, LOC100499194, LOC440900, MARCO, MIR4782, NIFK-AS1, PCDP1, PTPN4, RABL2A, RALB, RNU4ATAC, RPL23AP7, SCTR, SLC35F5, STEAP3, TFCP2L1, TMEM177, TMEM185B, TMEM37, WASH2P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553311
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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