A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6177486



Internal ID9154889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102692778..102696616hg38UCSC Ensembl
Outerchr10:102692741..102696666hg38UCSC Ensembl
Innerchr10:104452535..104456373hg19UCSC Ensembl
Outerchr10:104452498..104456423hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg383926
hg193926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668455
Supporting Variants
SamplesNA18615
Known GenesARL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6177486
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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