A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5908868



Internal ID8886271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33203712..33204001hg38UCSC Ensembl
chr10:33492640..33492929hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678844
Supporting Variants
SamplesNA18572
Known GenesNRP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5908868
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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