A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6257185



Internal ID9234588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25287925..25335031hg38UCSC Ensembl
Outerchr1:25287554..25335401hg38UCSC Ensembl
Innerchr1:25614416..25661522hg19UCSC Ensembl
Outerchr1:25614045..25661892hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3847848
hg1947848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657070
Supporting Variants
SamplesHG00158
Known GenesRHD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6257185
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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