A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5940032



Internal ID9609873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144326299..144333722hg38UCSC Ensembl
Outerchr6:144326142..144333875hg38UCSC Ensembl
Innerchr6:144647435..144654858hg19UCSC Ensembl
Outerchr6:144647278..144655011hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387734
hg197734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657131
Supporting Variants
SamplesNA19311
Known GenesUTRN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5940032
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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