A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13408158



Internal ID1074490
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619791
Supporting Variants
SamplesHG00699
Known GenesCCDC171
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13408158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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