A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636606



Internal ID6676713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57272529..57303422hg38UCSC Ensembl
chr15:57564727..57595620hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830894
hg1930894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15259147
SamplesHG02419
Known GenesLINC00926, TCF12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636606
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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