A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670380



Internal ID9936485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24180337..24569194hg38UCSC Ensembl
chr15:24425484..24814341hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38388858
hg19388858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv441e199
Supporting Variantsessv6591751
SamplesHG01173
Known GenesPWRN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670380
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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