A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5615317



Internal ID8592720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47514492..47585778hg38UCSC Ensembl
Outerchr10:47514116..47586148hg38UCSC Ensembl
Innerchr10:48913816..48984722hg19UCSC Ensembl
Outerchr10:48913445..48985092hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3872033
hg1971648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659652
Supporting Variants
SamplesHG00326
Known GenesBMS1P1, BMS1P5, GLUD1P7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5615317
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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