A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595925



Internal ID6636199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39314483..39353966hg38UCSC Ensembl
Innerchr3:39314483..39353966hg38UCSC Ensembl
Outerchr3:39313983..39354466hg38UCSC Ensembl
chr3:39355974..39395457hg19UCSC Ensembl
Innerchr3:39355974..39395457hg19UCSC Ensembl
Outerchr3:39355474..39395957hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3839484
hg1939484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987712, essv10987710, essv10987711
SamplesHG03111, NA18858, NA19835
Known GenesCCR8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595925
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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