A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635914



Internal ID7022711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24913053..24915241hg38UCSC Ensembl
Innerchr15:24913104..24915190hg38UCSC Ensembl
Outerchr15:24913002..24915292hg38UCSC Ensembl
chr15:25158200..25160388hg19UCSC Ensembl
Innerchr15:25158251..25160337hg19UCSC Ensembl
Outerchr15:25158149..25160439hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382189
hg192189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15186778
SamplesNA07347
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635914
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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