A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11360136



Internal ID1058683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15172128..15276959hg38UCSC Ensembl
Innerchr4:15172128..15276959hg38UCSC Ensembl
Outerchr4:15171628..15277459hg38UCSC Ensembl
chr4:15173752..15278583hg19UCSC Ensembl
Innerchr4:15173752..15278583hg19UCSC Ensembl
Outerchr4:15173252..15279083hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38104832
hg19104832
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599735
Supporting Variants
SamplesHG00683
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11360136
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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