A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10901963



Internal ID903779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3009752..3025488hg38UCSC Ensembl
Innerchr3:3010252..3024988hg38UCSC Ensembl
Outerchr3:3008752..3026488hg38UCSC Ensembl
chr3:3051436..3067172hg19UCSC Ensembl
Innerchr3:3051936..3066672hg19UCSC Ensembl
Outerchr3:3050436..3068172hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3815737
hg1915737
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595047
Supporting Variants
SamplesHG01412
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10901963
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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