A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3437650



Internal ID15284603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22502487..22506685hg38UCSC Ensembl
Innerchr15:22503487..22505685hg38UCSC Ensembl
Outerchr15:22501487..22507685hg38UCSC Ensembl
chr15:23366411..23370609hg19UCSC Ensembl
Innerchr15:23367411..23369609hg19UCSC Ensembl
Outerchr15:23365411..23371609hg19UCSC Ensembl
chr15:20917852..20922050hg18UCSC Ensembl
Innerchr15:20918852..20921050hg18UCSC Ensembl
Outerchr15:20916852..20923050hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384199
hg194199
hg184199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689696
SamplesNA19238
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3437650
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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