A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604072



Internal ID6991102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13610420..13611580hg38UCSC Ensembl
Innerchr5:13610449..13611551hg38UCSC Ensembl
Outerchr5:13610391..13611609hg38UCSC Ensembl
chr5:13610529..13611689hg19UCSC Ensembl
Innerchr5:13610558..13611660hg19UCSC Ensembl
Outerchr5:13610500..13611718hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11818011
SamplesNA20587
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604072
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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