A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631514



Internal ID7018323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23185195..23192439hg38UCSC Ensembl
Innerchr13:23185195..23192439hg38UCSC Ensembl
Outerchr13:23185156..23192588hg38UCSC Ensembl
chr13:23759334..23766578hg19UCSC Ensembl
Innerchr13:23759334..23766578hg19UCSC Ensembl
Outerchr13:23759295..23766727hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg387245
hg197245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14669425
SamplesHG03168
Known GenesSGCG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631514
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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