A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631784



Internal ID7018593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36671707..36672749hg38UCSC Ensembl
Innerchr13:36671707..36672749hg38UCSC Ensembl
Outerchr13:36671415..36672997hg38UCSC Ensembl
chr13:37245844..37246886hg19UCSC Ensembl
Innerchr13:37245844..37246886hg19UCSC Ensembl
Outerchr13:37245552..37247134hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14691665
SamplesHG00543
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631784
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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