A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637112



Internal ID7023906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85384885..85468079hg38UCSC Ensembl
chr15:85928116..86011310hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3883195
hg1983195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15314282, essv15314281, essv15314279, essv15314283, essv15314280
SamplesNA19917, NA19437, NA19043, HG03967, HG02684
Known GenesAKAP13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637112
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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