A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11176269



Internal ID6298318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146709659..146710502hg38UCSC Ensembl
Innerchr3:146709659..146710502hg38UCSC Ensembl
Outerchr3:146709383..146710771hg38UCSC Ensembl
chr3:146427446..146428289hg19UCSC Ensembl
Innerchr3:146427446..146428289hg19UCSC Ensembl
Outerchr3:146427170..146428558hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598102
Supporting Variants
SamplesNA19901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11176269
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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