A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628657



Internal ID7015481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14862341..14865213hg38UCSC Ensembl
Innerchr12:14862370..14865184hg38UCSC Ensembl
Outerchr12:14862312..14865242hg38UCSC Ensembl
chr12:15015275..15018147hg19UCSC Ensembl
Innerchr12:15015304..15018118hg19UCSC Ensembl
Outerchr12:15015246..15018176hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg382873
hg192873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14394078
SamplesHG03645
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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