A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636026



Internal ID6676135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30628576..30700028hg38UCSC Ensembl
chr15:30920779..30992231hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3871453
hg1971453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15203648, essv15203651, essv15203650, essv15203649
SamplesNA12287, NA06986, HG01973, HG02679
Known GenesARHGAP11B, LOC100288637
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636026
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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