A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660097



Internal ID9579516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:526035..1246034hg38UCSC Ensembl
Outerchr10:526001..1246069hg38UCSC Ensembl
Innerchr10:571975..1288086hg19UCSC Ensembl
Outerchr10:571941..1288121hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38720069
hg19716181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6382984
SamplesHG00376
Known GenesADARB2, DIP2C, GTPBP4, IDI1, IDI2, IDI2-AS1, LARP4B, LINC00200, MIR5699, PRR26, WDR37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660097
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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