A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602363



Internal ID6989397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136355409..136362825hg38UCSC Ensembl
Innerchr4:136355422..136362812hg38UCSC Ensembl
Outerchr4:136355396..136362838hg38UCSC Ensembl
chr4:137276564..137283980hg19UCSC Ensembl
Innerchr4:137276577..137283967hg19UCSC Ensembl
Outerchr4:137276551..137283993hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg387417
hg197417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11620987
SamplesHG03212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602363
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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