A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6260417



Internal ID9379905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63484721..63488983hg38UCSC Ensembl
Outerchr10:63484684..63489033hg38UCSC Ensembl
Innerchr10:65244481..65248743hg19UCSC Ensembl
Outerchr10:65244444..65248793hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384350
hg194350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674014
Supporting Variants
SamplesNA18572
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6260417
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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