A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665294



Internal ID9931399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30432373..30432895hg38UCSC Ensembl
Outerchr10:30432336..30432945hg38UCSC Ensembl
Innerchr10:30721302..30721824hg19UCSC Ensembl
Outerchr10:30721265..30721874hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5660785
SamplesNA18553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665294
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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