A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6455378



Internal ID8721402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15553833..15563139hg38UCSC Ensembl
Outerchr9:15553796..15563189hg38UCSC Ensembl
Innerchr9:15553831..15563137hg19UCSC Ensembl
Outerchr9:15553794..15563187hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg389394
hg199394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661119
Supporting Variants
SamplesHG00100
Known GenesCCDC171
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6455378
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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