A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636652



Internal ID7023446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60023769..60058386hg38UCSC Ensembl
Innerchr15:60023769..60058386hg38UCSC Ensembl
Outerchr15:60023269..60058886hg38UCSC Ensembl
chr15:60315968..60350585hg19UCSC Ensembl
Innerchr15:60315968..60350585hg19UCSC Ensembl
Outerchr15:60315468..60351085hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3834618
hg1934618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261137
SamplesNA20334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636652
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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