A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621769



Internal ID7008635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126631519..126632692hg38UCSC Ensembl
Innerchr9:126631523..126632688hg38UCSC Ensembl
Outerchr9:126631515..126632696hg38UCSC Ensembl
chr9:129393798..129394971hg19UCSC Ensembl
Innerchr9:129393802..129394967hg19UCSC Ensembl
Outerchr9:129393794..129394975hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13620907
SamplesHG00737
Known GenesLMX1B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621769
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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