A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3399845



Internal ID15246808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26154807..26154816hg38UCSC Ensembl
Innerchr1:26154788..26154835hg38UCSC Ensembl
Outerchr1:26154779..26154844hg38UCSC Ensembl
chr1:26481298..26481307hg19UCSC Ensembl
Innerchr1:26481279..26481326hg19UCSC Ensembl
Outerchr1:26481270..26481335hg19UCSC Ensembl
chr1:26353885..26353894hg18UCSC Ensembl
Innerchr1:26353913..26353866hg18UCSC Ensembl
Outerchr1:26353857..26353922hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7863685
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3399845
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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