A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636461



Internal ID6676568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51022583..51482654hg38UCSC Ensembl
Innerchr15:51022733..51482504hg38UCSC Ensembl
Outerchr15:51022433..51482804hg38UCSC Ensembl
chr15:51314780..51774851hg19UCSC Ensembl
Innerchr15:51314930..51774701hg19UCSC Ensembl
Outerchr15:51314630..51775001hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38460072
hg19460072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15248315
SamplesNA19000
Known GenesCYP19A1, DMXL2, GLDN, MIR4713, TNFAIP8L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636461
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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