A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586308



Internal ID6973829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67529755..67531131hg38UCSC Ensembl
Innerchr1:67529818..67531069hg38UCSC Ensembl
Outerchr1:67529693..67531194hg38UCSC Ensembl
chr1:67995438..67996814hg19UCSC Ensembl
Innerchr1:67995501..67996752hg19UCSC Ensembl
Outerchr1:67995376..67996877hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381377
hg191377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9958935
SamplesHG01599
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586308
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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