A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6505164



Internal ID8755016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44261792..44265773hg38UCSC Ensembl
Outerchr10:44261755..44265823hg38UCSC Ensembl
Innerchr10:44757240..44761221hg19UCSC Ensembl
Outerchr10:44757203..44761271hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384069
hg194069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658242
Supporting Variants
SamplesHG00143
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6505164
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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