A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9899583



Internal ID6524876
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585710
Supporting Variants
SamplesHG00675
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9899583
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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