A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5995504



Internal ID8930542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13671083..13671687hg38UCSC Ensembl
Outerchr6:13671046..13671737hg38UCSC Ensembl
Innerchr6:13671315..13671919hg19UCSC Ensembl
Outerchr6:13671278..13671969hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674410
Supporting Variants
SamplesHG00442
Known GenesRANBP9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5995504
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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