A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603864



Internal ID6990895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3957741..3970602hg38UCSC Ensembl
Innerchr5:3957743..3970600hg38UCSC Ensembl
Outerchr5:3957739..3970604hg38UCSC Ensembl
chr5:3957855..3970716hg19UCSC Ensembl
Innerchr5:3957857..3970714hg19UCSC Ensembl
Outerchr5:3957853..3970718hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3812862
hg1912862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11791623, essv11791624, essv11791622
SamplesHG00231, HG00318, HG01525
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603864
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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