A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585589



Internal ID6973110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28623130..28633634hg38UCSC Ensembl
Innerchr1:28623630..28633134hg38UCSC Ensembl
Outerchr1:28622130..28634634hg38UCSC Ensembl
chr1:28949642..28960146hg19UCSC Ensembl
Innerchr1:28950142..28959646hg19UCSC Ensembl
Outerchr1:28948642..28961146hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3810505
hg1910505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894791, essv9894790
SamplesHG02082, NA18537
Known GenesTAF12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585589
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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