A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585710



Internal ID6626025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34711686..34714117hg38UCSC Ensembl
Innerchr1:34711701..34714102hg38UCSC Ensembl
Outerchr1:34711671..34714132hg38UCSC Ensembl
chr1:35177287..35179718hg19UCSC Ensembl
Innerchr1:35177302..35179703hg19UCSC Ensembl
Outerchr1:35177272..35179733hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382432
hg192432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9899583
SamplesHG00675
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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