A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596034



Internal ID6983352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44483926..44492016hg38UCSC Ensembl
Innerchr3:44483963..44491979hg38UCSC Ensembl
Outerchr3:44483889..44492053hg38UCSC Ensembl
chr3:44525418..44533508hg19UCSC Ensembl
Innerchr3:44525455..44533471hg19UCSC Ensembl
Outerchr3:44525381..44533545hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388091
hg198091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10993612
SamplesHG01783
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596034
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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