A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8969342



Internal ID13757694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91409302..91409344hg38UCSC Ensembl
Innerchr15:91409316..91409327hg38UCSC Ensembl
Outerchr15:91409277..91409369hg38UCSC Ensembl
chr15:91952532..91952574hg19UCSC Ensembl
Innerchr15:91952546..91952557hg19UCSC Ensembl
Outerchr15:91952507..91952599hg19UCSC Ensembl
chr15:89753536..89753578hg18UCSC Ensembl
Innerchr15:89753561..89753550hg18UCSC Ensembl
Outerchr15:89753511..89753603hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38262
hg19262
hg18262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3392528
Supporting Variants
SamplesNA18498
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8969342
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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