A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636068



Internal ID7022864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32025041..32123390hg38UCSC Ensembl
chr15:32317244..32415591hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3898350
hg1998348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15206770, essv15206775, essv15206765, essv15206773, essv15206777, essv15206772, essv15206774, essv15206768, essv15206776, essv15206771, essv15206767, essv15206769, essv15206766
SamplesNA11830, NA18528, HG00244, NA12813, 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)esv3636068
Frequency
Sample Size2504
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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