A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586825



Internal ID6971997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93216732..93235801hg38UCSC Ensembl
Innerchr1:93217232..93235301hg38UCSC Ensembl
Outerchr1:93215732..93236801hg38UCSC Ensembl
chr1:93682289..93701358hg19UCSC Ensembl
Innerchr1:93682789..93700858hg19UCSC Ensembl
Outerchr1:93681289..93702358hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3819070
hg1919070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10022144
SamplesNA20581
Known GenesCCDC18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586825
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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