A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632011



Internal ID7018821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47697127..47707498hg38UCSC Ensembl
Innerchr13:47697127..47707498hg38UCSC Ensembl
Outerchr13:47696627..47707998hg38UCSC Ensembl
chr13:48271262..48281633hg19UCSC Ensembl
Innerchr13:48271262..48281633hg19UCSC Ensembl
Outerchr13:48270762..48282133hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3810372
hg1910372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14713885
SamplesHG02058
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632011
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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