A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585382



Internal ID6972906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18065029..18068350hg38UCSC Ensembl
Innerchr1:18065079..18068300hg38UCSC Ensembl
Outerchr1:18064979..18068400hg38UCSC Ensembl
chr1:18391523..18394844hg19UCSC Ensembl
Innerchr1:18391573..18394794hg19UCSC Ensembl
Outerchr1:18391473..18394894hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg383322
hg193322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9876434
SamplesHG01956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585382
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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