A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621849



Internal ID7008715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129986687..129988445hg38UCSC Ensembl
Innerchr9:129986737..129988395hg38UCSC Ensembl
Outerchr9:129986533..129988599hg38UCSC Ensembl
chr9:132748966..132750724hg19UCSC Ensembl
Innerchr9:132749016..132750674hg19UCSC Ensembl
Outerchr9:132748812..132750878hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381759
hg191759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13629177, essv13629178, essv13629181, essv13629187, essv13629179, essv13629184, essv13629183, essv13629188, essv13629182, essv13629186, essv13629185, essv13629180
SamplesNA19141, HG03057, NA19350, HG03100, NA19027, HG03120, HG01882, HG01890, NA19434, NA19072, HG02013, HG03445
Known GenesFNBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621849
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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