A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689680



Internal ID15020515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22552987..22559185hg38UCSC Ensembl
Innerchr15:22553987..22558185hg38UCSC Ensembl
Outerchr15:22551987..22560185hg38UCSC Ensembl
chr15:23313911..23320109hg19UCSC Ensembl
Innerchr15:23314911..23319109hg19UCSC Ensembl
Outerchr15:23312911..23321109hg19UCSC Ensembl
chr15:20865352..20871550hg18UCSC Ensembl
Innerchr15:20866352..20870550hg18UCSC Ensembl
Outerchr15:20864352..20872550hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386199
hg196199
hg186199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3385626
Supporting Variants
SamplesNA19238
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689680
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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