A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689678



Internal ID15095032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22530987..22559485hg38UCSC Ensembl
Innerchr15:22531987..22558485hg38UCSC Ensembl
Outerchr15:22529987..22560485hg38UCSC Ensembl
chr15:23313611..23342109hg19UCSC Ensembl
Innerchr15:23314611..23341109hg19UCSC Ensembl
Outerchr15:23312611..23343109hg19UCSC Ensembl
chr15:20865052..20893550hg18UCSC Ensembl
Innerchr15:20866052..20892550hg18UCSC Ensembl
Outerchr15:20864052..20894550hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3828499
hg1928499
hg1828499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3361141
Supporting Variants
SamplesNA19240
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689678
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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