A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636413



Internal ID7023207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48343211..48344555hg38UCSC Ensembl
Innerchr15:48343227..48344540hg38UCSC Ensembl
Outerchr15:48343196..48344571hg38UCSC Ensembl
chr15:48635408..48636752hg19UCSC Ensembl
Innerchr15:48635424..48636737hg19UCSC Ensembl
Outerchr15:48635393..48636768hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15243869
SamplesHG03713
Known GenesDUT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636413
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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