A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665226



Internal ID9584645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72102253..72106128hg38UCSC Ensembl
Outerchr10:72102096..72106281hg38UCSC Ensembl
Innerchr10:73862011..73865886hg19UCSC Ensembl
Outerchr10:73861854..73866039hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384186
hg194186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv154e199
Supporting Variantsessv6170909, essv6264572
SamplesNA19448, NA18909
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665226
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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