A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13436664



Internal ID497939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28533659..28735701hg38UCSC Ensembl
Innerchr9:28533704..28735657hg38UCSC Ensembl
Outerchr9:28533615..28735746hg38UCSC Ensembl
chr9:28533657..28735699hg19UCSC Ensembl
Innerchr9:28533702..28735655hg19UCSC Ensembl
Outerchr9:28533613..28735744hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38202043
hg19202043
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620170
Supporting Variants
SamplesHG00177
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13436664
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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