A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6076588



Internal ID9053991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1026538..1029659hg38UCSC Ensembl
Outerchr10:1026501..1029709hg38UCSC Ensembl
Innerchr10:1072478..1075599hg19UCSC Ensembl
Outerchr10:1072441..1075649hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383209
hg193209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673024
Supporting Variants
SamplesNA18619
Known GenesIDI2-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6076588
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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