A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604647



Internal ID6991675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33287915..33322746hg38UCSC Ensembl
Innerchr5:33287926..33322736hg38UCSC Ensembl
Outerchr5:33287905..33322757hg38UCSC Ensembl
chr5:33288021..33322852hg19UCSC Ensembl
Innerchr5:33288032..33322842hg19UCSC Ensembl
Outerchr5:33288011..33322863hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3834832
hg1934832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1089e214
Supporting Variantsessv11859361
SamplesHG03604
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604647
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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