A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6342899



Internal ID9796368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88916401..88922403hg38UCSC Ensembl
chr15:89459632..89465634hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386003
hg196003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669142
Supporting Variants
SamplesNA19818
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6342899
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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