A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636067



Internal ID7022863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31993123..32154020hg38UCSC Ensembl
chr15:32285326..32446221hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38160898
hg19160896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15206757, essv15206764, essv15206763, essv15206756, essv15206762, essv15206755, essv15206761, essv15206759, essv15206760, essv15206758
SamplesNA18528, HG00244, NA12813, HG03595, HG02260, HG01709, HG00141, HG03790, HG01377, HG00759
Known GenesCHRNA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636067
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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