A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672872



Internal ID9592291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1514579..1514969hg38UCSC Ensembl
Outerchr10:1514542..1515019hg38UCSC Ensembl
Innerchr10:1556774..1557164hg19UCSC Ensembl
Outerchr10:1556737..1557214hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5868696, essv6456354
SamplesHG00427, NA18549
Known GenesADARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672872
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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