A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636065



Internal ID7022861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31977391..32055670hg38UCSC Ensembl
chr15:32269594..32347873hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3878280
hg1978280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15206732, essv15206742, essv15206746, essv15206743, essv15206737, essv15206736, essv15206740, essv15206734, essv15206738, essv15206741, essv15206744, essv15206733, essv15206739, essv15206745, essv15206735
SamplesNA11830, NA18528, HG00244, NA12813, NA20278, HG00106, HG03595, HG02260, HG01709, NA18747, HG01512, HG03790, HG01894, HG01377, HG00759
Known GenesCHRNA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636065
Frequency
Sample Size2504
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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