A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636308



Internal ID7023104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44464998..44466244hg38UCSC Ensembl
Innerchr15:44464998..44466244hg38UCSC Ensembl
Outerchr15:44464665..44466519hg38UCSC Ensembl
chr15:44757196..44758442hg19UCSC Ensembl
Innerchr15:44757196..44758442hg19UCSC Ensembl
Outerchr15:44756863..44758717hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233235, essv15233236, essv15233234, essv15233243, essv15233240, essv15233242, essv15233241, essv15233237, essv15233238, essv15233233, essv15233239
SamplesNA20274, HG01389, NA20802, HG01070, HG01365, NA20759, HG00743, HG00101, HG01536, NA12043, HG01678
Known GenesCTDSPL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636308
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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