A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619791



Internal ID7006665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15699536..15728230hg38UCSC Ensembl
Innerchr9:15699536..15728230hg38UCSC Ensembl
Outerchr9:15699036..15728730hg38UCSC Ensembl
chr9:15699534..15728228hg19UCSC Ensembl
Innerchr9:15699534..15728228hg19UCSC Ensembl
Outerchr9:15699034..15728728hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3828695
hg1928695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13408158
SamplesHG00699
Known GenesCCDC171
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619791
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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