A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603941



Internal ID6990972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7929044..7930371hg38UCSC Ensembl
Innerchr5:7929057..7930359hg38UCSC Ensembl
Outerchr5:7929032..7930384hg38UCSC Ensembl
chr5:7929157..7930484hg19UCSC Ensembl
Innerchr5:7929170..7930472hg19UCSC Ensembl
Outerchr5:7929145..7930497hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11805117
SamplesHG04206
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603941
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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