A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637125



Internal ID7023919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85808038..85848377hg38UCSC Ensembl
Innerchr15:85808188..85848227hg38UCSC Ensembl
Outerchr15:85807888..85848527hg38UCSC Ensembl
chr15:86351269..86391608hg19UCSC Ensembl
Innerchr15:86351419..86391458hg19UCSC Ensembl
Outerchr15:86351119..86391758hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3840340
hg1940340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15315823
SamplesHG03461
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637125
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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