A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15339037



Internal ID5340853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98889499..98967530hg38UCSC Ensembl
Innerchr15:98889649..98967380hg38UCSC Ensembl
Outerchr15:98889349..98967680hg38UCSC Ensembl
chr15:99432728..99510759hg19UCSC Ensembl
Innerchr15:99432878..99510609hg19UCSC Ensembl
Outerchr15:99432578..99510909hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3878032
hg1978032
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637409
Supporting Variants
SamplesNA18977
Known GenesIGF1R
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15339037
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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