A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5959097



Internal ID9564475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15000174..15000982hg38UCSC Ensembl
Outerchr1:15000017..15001135hg38UCSC Ensembl
Innerchr1:15326670..15327478hg19UCSC Ensembl
Outerchr1:15326513..15327631hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381119
hg191119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676425
Supporting Variants
SamplesNA19108
Known GenesKAZN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5959097
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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