A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8673238



Internal ID15032642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74910691..74910748hg38UCSC Ensembl
Innerchr15:74910718..74910721hg38UCSC Ensembl
Outerchr15:74910661..74910778hg38UCSC Ensembl
chr15:75203032..75203089hg19UCSC Ensembl
Innerchr15:75203059..75203062hg19UCSC Ensembl
Outerchr15:75203002..75203119hg19UCSC Ensembl
chr15:72990085..72990142hg18UCSC Ensembl
Innerchr15:72990115..72990112hg18UCSC Ensembl
Outerchr15:72990055..72990172hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38195
hg19195
hg18195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3365571
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8673238
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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