A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13571502



Internal ID3573318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94880452..94886100hg38UCSC Ensembl
Innerchr9:94880491..94886061hg38UCSC Ensembl
Outerchr9:94880413..94886139hg38UCSC Ensembl
chr9:97642734..97648382hg19UCSC Ensembl
Innerchr9:97642773..97648343hg19UCSC Ensembl
Outerchr9:97642695..97648421hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385649
hg195649
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621140
Supporting Variants
SamplesHG02479
Known GenesC9orf3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13571502
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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