A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6020327



Internal ID8924441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89040497..89053020hg38UCSC Ensembl
Outerchr15:89040325..89053205hg38UCSC Ensembl
Innerchr15:89583728..89596251hg19UCSC Ensembl
Outerchr15:89583556..89596436hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812881
hg1912881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663539
Supporting Variants
SamplesHG00428
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6020327
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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