A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670261



Internal ID9936366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72110530..72112476hg38UCSC Ensembl
Outerchr10:72110493..72112526hg38UCSC Ensembl
Innerchr10:73870288..73872234hg19UCSC Ensembl
Outerchr10:73870251..73872284hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6567002
SamplesNA12749
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670261
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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