A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11073028



Internal ID4784714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96063664..96066507hg38UCSC Ensembl
Innerchr3:96063684..96066488hg38UCSC Ensembl
Outerchr3:96063645..96066527hg38UCSC Ensembl
chr3:95782508..95785351hg19UCSC Ensembl
Innerchr3:95782528..95785332hg19UCSC Ensembl
Outerchr3:95782489..95785371hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg382844
hg192844
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597064
Supporting Variants
SamplesNA11918
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11073028
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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