A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631752



Internal ID7018561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34504892..34506257hg38UCSC Ensembl
Innerchr13:34504892..34506257hg38UCSC Ensembl
Outerchr13:34504800..34506351hg38UCSC Ensembl
chr13:35079029..35080394hg19UCSC Ensembl
Innerchr13:35079029..35080394hg19UCSC Ensembl
Outerchr13:35078937..35080488hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14688227
SamplesHG01947
Known GenesLINC00457
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631752
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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