A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6401932



Internal ID9124665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68583900..68586006hg38UCSC Ensembl
Outerchr9:68583529..68586376hg38UCSC Ensembl
Innerchr9:71198816..71200922hg19UCSC Ensembl
Outerchr9:71198445..71201292hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674110
Supporting Variants
SamplesHG01140
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6401932
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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