A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6319919



Internal ID9297322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110030202..110031031hg38UCSC Ensembl
Outerchr10:110030045..110031184hg38UCSC Ensembl
Innerchr10:111789960..111790789hg19UCSC Ensembl
Outerchr10:111789803..111790942hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676886
Supporting Variants
SamplesNA18615
Known GenesADD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6319919
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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