A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676009



Internal ID9595428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132540992..132541108hg38UCSC Ensembl
chr10:134354496..134354612hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6251515, essv6265179, essv6364850
SamplesHG01107, NA18945, HG01108
Known GenesINPP5A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676009
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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