A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13660492



Internal ID3662308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137634104..137729031hg38UCSC Ensembl
Innerchr9:137634162..137728974hg38UCSC Ensembl
Outerchr9:137634047..137729089hg38UCSC Ensembl
chr9:140528556..140623483hg19UCSC Ensembl
Innerchr9:140528614..140623426hg19UCSC Ensembl
Outerchr9:140528499..140623541hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3894928
hg1994928
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622038
Supporting Variants
SamplesHG01342
Known GenesEHMT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13660492
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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