A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636837



Internal ID7023631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70456207..70457036hg38UCSC Ensembl
Innerchr15:70456207..70457036hg38UCSC Ensembl
Outerchr15:70456023..70457366hg38UCSC Ensembl
chr15:70748546..70749375hg19UCSC Ensembl
Innerchr15:70748546..70749375hg19UCSC Ensembl
Outerchr15:70748362..70749705hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15283138, essv15283137, essv15283139
SamplesHG02322, HG01101, HG01107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636837
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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