A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11158469



Internal ID2459522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137060290..137063457hg38UCSC Ensembl
Innerchr3:137060298..137063450hg38UCSC Ensembl
Outerchr3:137060283..137063465hg38UCSC Ensembl
chr3:136779132..136782299hg19UCSC Ensembl
Innerchr3:136779140..136782292hg19UCSC Ensembl
Outerchr3:136779125..136782307hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383168
hg193168
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597896
Supporting Variants
SamplesHG02165
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11158469
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer