A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637111



Internal ID7023905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85291627..85464874hg38UCSC Ensembl
Innerchr15:85291777..85464724hg38UCSC Ensembl
Outerchr15:85291477..85465024hg38UCSC Ensembl
chr15:85834858..86008105hg19UCSC Ensembl
Innerchr15:85835008..86007955hg19UCSC Ensembl
Outerchr15:85834708..86008255hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38173248
hg19173248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15314278, essv15314275, essv15314274, essv15314277, essv15314276
SamplesHG04038, NA19917, NA19043, HG03967, HG02684
Known GenesAKAP13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637111
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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