A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636116



Internal ID6676225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34429035..34544625hg38UCSC Ensembl
chr15:34721236..34836826hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38115591
hg19115591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15211048, essv15211055, essv15211081, essv15211052, essv15211060, essv15211080, essv15211074, essv15211049, essv15211057, essv15211084, essv15211061, essv15211085, essv15211078, essv15211064, essv15211069, essv15211053, essv15211051, essv15211075, essv15211045, essv15211066, essv15211077, essv15211070, essv15211054, essv15211086, essv15211062, essv15211073, essv15211082, essv15211083, essv15211050, essv15211046, essv15211076, essv15211063, essv15211056, essv15211079, essv15211047, essv15211067, essv15211071, essv15211059, essv15211065, essv15211068, essv15211058, essv15211087, essv15211072
SamplesNA18745, HG02574, HG02628, NA19066, NA18592, HG03753, HG02061, NA20507, HG02589, NA18526, HG01694, HG01513, NA19201, HG01459, HG03604, HG02130, HG00736, HG01848, NA18964, HG03520, HG01519, HG04020, HG02882, NA19007, NA18934, NA18956, HG01882, HG02144, NA18879, NA19740, HG03024, HG02256, NA19035, HG02282, NA18535, HG01977, NA20281, HG02771, HG02974, NA18609, NA19096, HG03611, HG02465
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636116
Frequency
Sample Size2504
Observed Gain43
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer