A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620382



Internal ID7007253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35662903..35664509hg38UCSC Ensembl
Innerchr9:35662911..35664502hg38UCSC Ensembl
Outerchr9:35662896..35664517hg38UCSC Ensembl
chr9:35662900..35664506hg19UCSC Ensembl
Innerchr9:35662908..35664499hg19UCSC Ensembl
Outerchr9:35662893..35664514hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381607
hg191607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13459411, essv13459412, essv13459414, essv13459410, essv13459409, essv13459415, essv13459416, essv13459413
SamplesNA19648, HG02727, HG03926, NA12058, HG02792, HG02789, HG00155, NA12830
Known GenesARHGEF39
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620382
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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