A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603973



Internal ID6991003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9375418..9410785hg38UCSC Ensembl
Innerchr5:9375418..9410785hg38UCSC Ensembl
Outerchr5:9374918..9411285hg38UCSC Ensembl
chr5:9375530..9410897hg19UCSC Ensembl
Innerchr5:9375530..9410897hg19UCSC Ensembl
Outerchr5:9375030..9411397hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3835368
hg1935368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11807184
SamplesHG04099
Known GenesSEMA5A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603973
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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