A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632951



Internal ID7019761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84531509..84532363hg38UCSC Ensembl
Innerchr13:84531512..84532360hg38UCSC Ensembl
Outerchr13:84531506..84532366hg38UCSC Ensembl
chr13:85105644..85106498hg19UCSC Ensembl
Innerchr13:85105647..85106495hg19UCSC Ensembl
Outerchr13:85105641..85106501hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822527
SamplesHG02375
Known GenesLINC00333
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632951
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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