A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604605



Internal ID6991633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32321396..32323177hg38UCSC Ensembl
Innerchr5:32321402..32323171hg38UCSC Ensembl
Outerchr5:32321390..32323183hg38UCSC Ensembl
chr5:32321502..32323283hg19UCSC Ensembl
Innerchr5:32321508..32323277hg19UCSC Ensembl
Outerchr5:32321496..32323289hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381782
hg191782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11855424
SamplesNA21144
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604605
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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