A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665093



Internal ID9931198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97683862..97684690hg38UCSC Ensembl
chr10:99443619..99444447hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5490015, essv5873157, essv5687060, essv5758545, essv5932684, essv6266377
SamplesNA19404, NA19317, NA19449, NA19469, NA19470, NA19468
Known GenesAVPI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665093
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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