A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636977



Internal ID7023771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77957698..78017979hg38UCSC Ensembl
chr15:78250040..78310321hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3860282
hg1960282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15301209, essv15301210, essv15301211, essv15301212
SamplesHG01366, HG01353, HG01345, HG01148
Known GenesLOC91450, TBC1D2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636977
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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