A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631764



Internal ID7018573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35415558..35423461hg38UCSC Ensembl
Innerchr13:35415558..35423461hg38UCSC Ensembl
Outerchr13:35415058..35423961hg38UCSC Ensembl
chr13:35989695..35997598hg19UCSC Ensembl
Innerchr13:35989695..35997598hg19UCSC Ensembl
Outerchr13:35989195..35998098hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387904
hg197904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14688580, essv14688579
SamplesNA18947, NA19130
Known GenesNBEA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631764
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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