A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604102



Internal ID6991132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14980086..15134257hg38UCSC Ensembl
Innerchr5:14980236..15134107hg38UCSC Ensembl
Outerchr5:14979936..15134407hg38UCSC Ensembl
chr5:14980195..15134366hg19UCSC Ensembl
Innerchr5:14980345..15134216hg19UCSC Ensembl
Outerchr5:14980045..15134516hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38154172
hg19154172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11818540
SamplesHG02808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604102
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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