A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633467



Internal ID7020276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106527252..106532742hg38UCSC Ensembl
chr13:107179600..107185090hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14890308, essv14890307
SamplesHG00257, HG03873
Known GenesEFNB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633467
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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