A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620335



Internal ID7007206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33871811..34738198hg38UCSC Ensembl
Innerchr9:33871961..34738048hg38UCSC Ensembl
Outerchr9:33871661..34738348hg38UCSC Ensembl
chr9:33871809..34738195hg19UCSC Ensembl
Innerchr9:33871959..34738045hg19UCSC Ensembl
Outerchr9:33871659..34738345hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38866388
hg19866387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13458032
SamplesHG01602
Known GenesARID3C, C9orf24, CCL19, CCL21, CCL27, CNTFR, CNTFR-AS1, DCAF12, DCTN3, DNAI1, ENHO, FAM205A, FAM219A, GALT, IL11RA, KIAA1161, KIF24, NUDT2, RPP25L, SIGMAR1, SNORD121A, SNORD121B, UBAP1, UBAP2, UBE2R2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620335
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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