A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7744585



Internal ID13762747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91409304..91409305hg38UCSC Ensembl
Innerchr15:91409259..91409350hg38UCSC Ensembl
Outerchr15:91409258..91409351hg38UCSC Ensembl
chr15:91952534..91952535hg19UCSC Ensembl
Innerchr15:91952489..91952580hg19UCSC Ensembl
Outerchr15:91952488..91952581hg19UCSC Ensembl
chr15:89753538..89753539hg18UCSC Ensembl
Innerchr15:89753584..89753493hg18UCSC Ensembl
Outerchr15:89753492..89753585hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305908
Supporting Variants
SamplesNA18498
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7744585
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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