A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6236001



Internal ID9113511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32711215..32729831hg38UCSC Ensembl
Outerchr9:32711175..32729892hg38UCSC Ensembl
Innerchr9:32711213..32729829hg19UCSC Ensembl
Outerchr9:32711173..32729890hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3818718
hg1918718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671053
Supporting Variants
SamplesHG01111
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6236001
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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