A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600103



Internal ID6987147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32069353..32072878hg38UCSC Ensembl
Innerchr4:32069353..32072878hg38UCSC Ensembl
Outerchr4:32069151..32072988hg38UCSC Ensembl
chr4:32070975..32074500hg19UCSC Ensembl
Innerchr4:32070975..32074500hg19UCSC Ensembl
Outerchr4:32070773..32074610hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg383526
hg193526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11387948
SamplesHG04214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600103
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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