A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5920944



Internal ID9708296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105784438..105785894hg38UCSC Ensembl
Outerchr8:105784067..105786264hg38UCSC Ensembl
Innerchr8:106796666..106798122hg19UCSC Ensembl
Outerchr8:106796295..106798492hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382198
hg192198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676076
Supporting Variants
SamplesNA19461
Known GenesZFPM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5920944
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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