A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619282



Internal ID7006160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2141570..2142739hg38UCSC Ensembl
Innerchr9:2141570..2142739hg38UCSC Ensembl
Outerchr9:2141336..2142970hg38UCSC Ensembl
chr9:2141570..2142739hg19UCSC Ensembl
Innerchr9:2141570..2142739hg19UCSC Ensembl
Outerchr9:2141336..2142970hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13378886, essv13378885
SamplesHG00620, NA20772
Known GenesSMARCA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619282
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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