A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585681



Internal ID6625996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33148849..33150994hg38UCSC Ensembl
Innerchr1:33148849..33150994hg38UCSC Ensembl
Outerchr1:33148667..33151259hg38UCSC Ensembl
chr1:33614450..33616595hg19UCSC Ensembl
Innerchr1:33614450..33616595hg19UCSC Ensembl
Outerchr1:33614268..33616860hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382146
hg192146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9896484
SamplesHG03258
Known GenesTRIM62
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585681
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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