A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5605587



Internal ID8893304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21396188..21398090hg38UCSC Ensembl
Outerchr10:21396151..21398140hg38UCSC Ensembl
Innerchr10:21685117..21687019hg19UCSC Ensembl
Outerchr10:21685080..21687069hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661682
Supporting Variants
SamplesHG00342
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5605587
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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