A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10954681



Internal ID1646533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26311968..26361505hg38UCSC Ensembl
Innerchr3:26311968..26361505hg38UCSC Ensembl
Outerchr3:26311468..26362005hg38UCSC Ensembl
chr3:26353459..26402996hg19UCSC Ensembl
Innerchr3:26353459..26402996hg19UCSC Ensembl
Outerchr3:26352959..26403496hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3849538
hg1949538
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595631
Supporting Variants
SamplesHG01515
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10954681
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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