A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585678



Internal ID6625993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32808106..32811771hg38UCSC Ensembl
Innerchr1:32808119..32811759hg38UCSC Ensembl
Outerchr1:32808094..32811784hg38UCSC Ensembl
chr1:33273707..33277372hg19UCSC Ensembl
Innerchr1:33273720..33277360hg19UCSC Ensembl
Outerchr1:33273695..33277385hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9896470
SamplesHG00132
Known GenesYARS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585678
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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