A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604933



Internal ID6991961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44919309..44934465hg38UCSC Ensembl
Innerchr5:44919329..44934445hg38UCSC Ensembl
Outerchr5:44919289..44934485hg38UCSC Ensembl
chr5:44919411..44934567hg19UCSC Ensembl
Innerchr5:44919431..44934547hg19UCSC Ensembl
Outerchr5:44919391..44934587hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3815157
hg1915157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11890257
SamplesNA20861
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604933
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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